BR112013016191B1 - compostos com capacidade de liberar compostos de fragrância, seu uso, método de geração por oxidação ao ar espontânea de um composto de carbonila e produto de consumo - Google Patents
compostos com capacidade de liberar compostos de fragrância, seu uso, método de geração por oxidação ao ar espontânea de um composto de carbonila e produto de consumo Download PDFInfo
- Publication number
- BR112013016191B1 BR112013016191B1 BR112013016191-4A BR112013016191A BR112013016191B1 BR 112013016191 B1 BR112013016191 B1 BR 112013016191B1 BR 112013016191 A BR112013016191 A BR 112013016191A BR 112013016191 B1 BR112013016191 B1 BR 112013016191B1
- Authority
- BR
- Brazil
- Prior art keywords
- alkyl
- enyl
- methyl
- benzene
- equiv
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 136
- 238000000034 method Methods 0.000 title claims description 17
- 150000001728 carbonyl compounds Chemical class 0.000 title claims description 7
- 230000003647 oxidation Effects 0.000 title claims description 6
- 238000007254 oxidation reaction Methods 0.000 title claims description 6
- 230000002269 spontaneous effect Effects 0.000 title claims description 5
- 239000003205 fragrance Substances 0.000 title abstract description 25
- -1 2- ( 2- (4-methylcyclohex-3-en-1-yl) propyl) cyclopent-1-ylidene Chemical group 0.000 claims description 72
- 229910052739 hydrogen Inorganic materials 0.000 claims description 48
- 239000001257 hydrogen Substances 0.000 claims description 48
- 239000000203 mixture Substances 0.000 claims description 41
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 40
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 31
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 30
- 150000001299 aldehydes Chemical class 0.000 claims description 30
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 24
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 125000003342 alkenyl group Chemical group 0.000 claims description 18
- 125000001033 ether group Chemical group 0.000 claims description 17
- 150000002576 ketones Chemical class 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 13
- 150000002431 hydrogen Chemical group 0.000 claims description 13
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 claims description 11
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 claims description 11
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 claims description 10
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 10
- 150000002430 hydrocarbons Chemical group 0.000 claims description 10
- 239000002243 precursor Substances 0.000 claims description 10
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 claims description 9
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 8
- 229920002554 vinyl polymer Chemical group 0.000 claims description 8
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 claims description 6
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 6
- 125000001118 alkylidene group Chemical group 0.000 claims description 6
- 238000004140 cleaning Methods 0.000 claims description 6
- 150000003254 radicals Chemical class 0.000 claims description 6
- UCSIFMPORANABL-UHFFFAOYSA-N 3,7-dimethyloctanal Chemical compound CC(C)CCCC(C)CC=O UCSIFMPORANABL-UHFFFAOYSA-N 0.000 claims description 5
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 claims description 5
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims description 4
- FSKGFRBHGXIDSA-UHFFFAOYSA-N 2-(4-propan-2-ylphenyl)acetaldehyde Chemical compound CC(C)C1=CC=C(CC=O)C=C1 FSKGFRBHGXIDSA-UHFFFAOYSA-N 0.000 claims description 4
- WTPYRCJDOZVZON-UHFFFAOYSA-N 3,5,5-Trimethylhexanal Chemical compound O=CCC(C)CC(C)(C)C WTPYRCJDOZVZON-UHFFFAOYSA-N 0.000 claims description 4
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 claims description 4
- WTWBUQJHJGUZCY-UHFFFAOYSA-N cuminaldehyde Chemical compound CC(C)C1=CC=C(C=O)C=C1 WTWBUQJHJGUZCY-UHFFFAOYSA-N 0.000 claims description 4
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 claims description 4
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 claims description 4
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 claims description 4
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 claims description 4
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 claims description 4
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- VWMVAQHMFFZQGD-UHFFFAOYSA-N p-Hydroxybenzyl acetone Natural products CC(=O)CC1=CC=C(O)C=C1 VWMVAQHMFFZQGD-UHFFFAOYSA-N 0.000 claims description 4
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 4
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 claims description 4
- NJGBTKGETPDVIK-UHFFFAOYSA-N raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 claims description 4
- BGEHHAVMRVXCGR-UHFFFAOYSA-N tridecanal Chemical compound CCCCCCCCCCCCC=O BGEHHAVMRVXCGR-UHFFFAOYSA-N 0.000 claims description 4
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 claims description 4
- PSQYTAPXSHCGMF-BQYQJAHWSA-N β-ionone Chemical compound CC(=O)\C=C\C1=C(C)CCCC1(C)C PSQYTAPXSHCGMF-BQYQJAHWSA-N 0.000 claims description 4
- 239000001304 (2R)-2,6-dimethylhept-5-enal Substances 0.000 claims description 3
- CIXAYNMKFFQEFU-UHFFFAOYSA-N (4-Methylphenyl)acetaldehyde Chemical compound CC1=CC=C(CC=O)C=C1 CIXAYNMKFFQEFU-UHFFFAOYSA-N 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims description 3
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 claims description 3
- QEUCRVAOUUCNJV-UHFFFAOYSA-N 1,2-dimethoxy-4-[4-(3-propan-2-ylphenyl)pent-1-enyl]benzene Chemical compound C1=C(OC)C(OC)=CC=C1C=CCC(C)C1=CC=CC(C(C)C)=C1 QEUCRVAOUUCNJV-UHFFFAOYSA-N 0.000 claims description 3
- UYIUDXMQYWPVAY-UHFFFAOYSA-N 1-(2,2-dimethyl-5-phenylpent-3-enyl)-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1CC(C)(C)C=CCC1=CC=CC=C1 UYIUDXMQYWPVAY-UHFFFAOYSA-N 0.000 claims description 3
- AOTOGNPVLZNOPY-UHFFFAOYSA-N 1-(6-phenylhex-4-en-2-yl)-3-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC(C(C)CC=CCC=2C=CC=CC=2)=C1 AOTOGNPVLZNOPY-UHFFFAOYSA-N 0.000 claims description 3
- DUPAQRQDWOVTCS-RQDYCKPOSA-N 1-[(6e)-dodeca-2,6-dienyl]-4-methoxybenzene Chemical compound CCCCC\C=C\CCC=CCC1=CC=C(OC)C=C1 DUPAQRQDWOVTCS-RQDYCKPOSA-N 0.000 claims description 3
- VAYVNWUYGAJDOE-RQDYCKPOSA-N 1-[(6e)-dodeca-2,6-dienyl]-4-methylbenzene Chemical compound CCCCC\C=C\CCC=CCC1=CC=C(C)C=C1 VAYVNWUYGAJDOE-RQDYCKPOSA-N 0.000 claims description 3
- KZXNEQMEXJAKKD-UHFFFAOYSA-N 1-methoxy-4-(3-methyldodec-1-enyl)benzene Chemical compound CCCCCCCCCC(C)C=CC1=CC=C(OC)C=C1 KZXNEQMEXJAKKD-UHFFFAOYSA-N 0.000 claims description 3
- UJWBRAKSLNDKPA-UHFFFAOYSA-N 1-methoxy-4-(4-methyltridec-2-enyl)benzene Chemical compound CCCCCCCCCC(C)C=CCC1=CC=C(OC)C=C1 UJWBRAKSLNDKPA-UHFFFAOYSA-N 0.000 claims description 3
- KSMUXDGHJKQJPN-RQDYCKPOSA-N 1-methoxy-4-[(5e)-undeca-1,5-dienyl]benzene Chemical compound CCCCC\C=C\CCC=CC1=CC=C(OC)C=C1 KSMUXDGHJKQJPN-RQDYCKPOSA-N 0.000 claims description 3
- TXQRNOUJBIVHLD-UHFFFAOYSA-N 1-methoxy-4-[4-(3-propan-2-ylphenyl)pent-1-enyl]benzene Chemical compound C1=CC(OC)=CC=C1C=CCC(C)C1=CC=CC(C(C)C)=C1 TXQRNOUJBIVHLD-UHFFFAOYSA-N 0.000 claims description 3
- DWGHUWXJHKXZNA-UHFFFAOYSA-N 1-methoxy-4-[5-(3-propan-2-ylphenyl)hex-2-enyl]benzene Chemical compound C1=CC(OC)=CC=C1CC=CCC(C)C1=CC=CC(C(C)C)=C1 DWGHUWXJHKXZNA-UHFFFAOYSA-N 0.000 claims description 3
- GOCMOBASIPUBEQ-UHFFFAOYSA-N 1-methyl-4-(4-methyltridec-2-enyl)benzene Chemical compound CCCCCCCCCC(C)C=CCC1=CC=C(C)C=C1 GOCMOBASIPUBEQ-UHFFFAOYSA-N 0.000 claims description 3
- DZYXWOPEVZIZOH-UHFFFAOYSA-N 1-tert-butyl-4-(2-methyl-5-phenylpent-3-enyl)benzene Chemical compound C=1C=CC=CC=1CC=CC(C)CC1=CC=C(C(C)(C)C)C=C1 DZYXWOPEVZIZOH-UHFFFAOYSA-N 0.000 claims description 3
- PQPYOGLSYULKRP-UHFFFAOYSA-N 1-tert-butyl-4-[2-methyl-5-(4-methylphenyl)pent-3-enyl]benzene Chemical compound C=1C=C(C)C=CC=1CC=CC(C)CC1=CC=C(C(C)(C)C)C=C1 PQPYOGLSYULKRP-UHFFFAOYSA-N 0.000 claims description 3
- YGTCEHBSRXHZFW-UHFFFAOYSA-N 1-tert-butyl-4-[4-(4-methoxyphenyl)-2-methylbut-3-enyl]benzene Chemical compound C1=CC(OC)=CC=C1C=CC(C)CC1=CC=C(C(C)(C)C)C=C1 YGTCEHBSRXHZFW-UHFFFAOYSA-N 0.000 claims description 3
- ZUOMFIQHUUWQEU-UHFFFAOYSA-N 1-tert-butyl-4-[5-(4-methoxyphenyl)-2-methylpent-3-enyl]benzene Chemical compound C1=CC(OC)=CC=C1CC=CC(C)CC1=CC=C(C(C)(C)C)C=C1 ZUOMFIQHUUWQEU-UHFFFAOYSA-N 0.000 claims description 3
- MZZRKEIUNOYYDF-UHFFFAOYSA-N 2,4-dimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1C=C(C)CCC1C=O MZZRKEIUNOYYDF-UHFFFAOYSA-N 0.000 claims description 3
- NXTMGVQDFYDTMX-UHFFFAOYSA-N 2-(4-methyltridec-2-en-2-yl)naphthalene Chemical compound C1=CC=CC2=CC(C(C)=CC(C)CCCCCCCCC)=CC=C21 NXTMGVQDFYDTMX-UHFFFAOYSA-N 0.000 claims description 3
- REJVAHLIIJLJJB-UHFFFAOYSA-N 2-(4-methyltridec-2-enyl)naphthalene Chemical compound C1=CC=CC2=CC(CC=CC(C)CCCCCCCCC)=CC=C21 REJVAHLIIJLJJB-UHFFFAOYSA-N 0.000 claims description 3
- UABARRYYLZLXFQ-UHFFFAOYSA-N 2-(5,7,7-trimethyloct-2-en-2-yl)naphthalene Chemical compound C1=CC=CC2=CC(C(C)=CCC(C)CC(C)(C)C)=CC=C21 UABARRYYLZLXFQ-UHFFFAOYSA-N 0.000 claims description 3
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 claims description 3
- FWTGHNUSSMOOHX-NZHODUKLSA-N 2-[(11e)-trideca-2,11-dien-2-yl]naphthalene Chemical compound C1=CC=CC2=CC(C(C)=CCCCCCCC/C=C/C)=CC=C21 FWTGHNUSSMOOHX-NZHODUKLSA-N 0.000 claims description 3
- SFZUMDAQDKNGGR-OUXDSOEMSA-N 2-[(6e)-dodeca-2,6-dien-2-yl]naphthalene Chemical compound C1=CC=CC2=CC(C(C)=CCC/C=C/CCCCC)=CC=C21 SFZUMDAQDKNGGR-OUXDSOEMSA-N 0.000 claims description 3
- KNHGOYVXAHUDHP-UHFFFAOYSA-N 2-[2-(4-methylcyclohex-3-en-1-yl)propyl]cyclopentan-1-one Chemical compound C1CC(C)=CCC1C(C)CC1CCCC1=O KNHGOYVXAHUDHP-UHFFFAOYSA-N 0.000 claims description 3
- VSJZJBVOENMSRL-UHFFFAOYSA-N 2-[4-(2-methylbutan-2-yl)cyclohexyl]acetaldehyde Chemical compound CCC(C)(C)C1CCC(CC=O)CC1 VSJZJBVOENMSRL-UHFFFAOYSA-N 0.000 claims description 3
- DKZCDROPRPTSPC-UHFFFAOYSA-N 2-[4-(4-methoxyphenyl)but-2-en-2-yl]naphthalene Chemical compound C1=CC(OC)=CC=C1CC=C(C)C1=CC=C(C=CC=C2)C2=C1 DKZCDROPRPTSPC-UHFFFAOYSA-N 0.000 claims description 3
- SJWNHAXIZWAFOH-UHFFFAOYSA-N 2-[5-(3-propan-2-ylphenyl)hex-2-en-2-yl]naphthalene Chemical compound CC(C)C1=CC=CC(C(C)CC=C(C)C=2C=C3C=CC=CC3=CC=2)=C1 SJWNHAXIZWAFOH-UHFFFAOYSA-N 0.000 claims description 3
- HWZFXDCEAQCFDY-UHFFFAOYSA-N 2-ethoxy-4-(3-methyldodec-1-enyl)phenol Chemical compound CCCCCCCCCC(C)C=CC1=CC=C(O)C(OCC)=C1 HWZFXDCEAQCFDY-UHFFFAOYSA-N 0.000 claims description 3
- PFOAAUACUMURSN-UHFFFAOYSA-N 2-ethoxy-4-(3-phenylprop-1-enyl)phenol Chemical compound C1=C(O)C(OCC)=CC(C=CCC=2C=CC=CC=2)=C1 PFOAAUACUMURSN-UHFFFAOYSA-N 0.000 claims description 3
- NNACZGJXARUDAC-UHFFFAOYSA-N 2-ethoxy-4-[3-(4-methoxyphenyl)prop-1-enyl]phenol Chemical compound C1=C(O)C(OCC)=CC(C=CCC=2C=CC(OC)=CC=2)=C1 NNACZGJXARUDAC-UHFFFAOYSA-N 0.000 claims description 3
- PEMWPSNVRCCJEF-UHFFFAOYSA-N 2-ethoxy-4-[3-(4-methylphenyl)prop-1-enyl]phenol Chemical compound C1=C(O)C(OCC)=CC(C=CCC=2C=CC(C)=CC=2)=C1 PEMWPSNVRCCJEF-UHFFFAOYSA-N 0.000 claims description 3
- HPOLMMDGJCOVPT-UHFFFAOYSA-N 2-ethoxy-4-[4-(3-propan-2-ylphenyl)pent-1-enyl]phenol Chemical compound C1=C(O)C(OCC)=CC(C=CCC(C)C=2C=C(C=CC=2)C(C)C)=C1 HPOLMMDGJCOVPT-UHFFFAOYSA-N 0.000 claims description 3
- MKSARIDKCHNUPI-UHFFFAOYSA-N 2-ethoxy-4-[4-(4-hydroxyphenyl)-2-methylbut-1-enyl]phenol Chemical compound C1=C(O)C(OCC)=CC(C=C(C)CCC=2C=CC(O)=CC=2)=C1 MKSARIDKCHNUPI-UHFFFAOYSA-N 0.000 claims description 3
- KQPOAOFGDJVJIB-UHFFFAOYSA-N 2-ethoxy-4-[[2-[2-(4-methylcyclohex-3-en-1-yl)propyl]cyclopentylidene]methyl]phenol Chemical compound C1=C(O)C(OCC)=CC(C=C2C(CCC2)CC(C)C2CC=C(C)CC2)=C1 KQPOAOFGDJVJIB-UHFFFAOYSA-N 0.000 claims description 3
- PMVDYAQAPLAXSY-UHFFFAOYSA-N 3-(2-oxopropyl)-2-pentylcyclopentan-1-one Chemical compound CCCCCC1C(CC(C)=O)CCC1=O PMVDYAQAPLAXSY-UHFFFAOYSA-N 0.000 claims description 3
- DXBXUMSLKADPEV-UHFFFAOYSA-N 3-(3-tert-butylcyclohexyl)propanal Chemical compound CC(C)(C)C1CCCC(CCC=O)C1 DXBXUMSLKADPEV-UHFFFAOYSA-N 0.000 claims description 3
- JFTSYAALCNQOKO-UHFFFAOYSA-N 3-(4-ethylphenyl)-2,2-dimethylpropanal Chemical compound CCC1=CC=C(CC(C)(C)C=O)C=C1 JFTSYAALCNQOKO-UHFFFAOYSA-N 0.000 claims description 3
- VLFBSPUPYFTTNF-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2-methylpropanal Chemical compound COC1=CC=C(CC(C)C=O)C=C1 VLFBSPUPYFTTNF-UHFFFAOYSA-N 0.000 claims description 3
- JRJBVWJSTHECJK-PKNBQFBNSA-N 3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one Chemical compound CC(=O)C(\C)=C\C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-PKNBQFBNSA-N 0.000 claims description 3
- TZJLGGWGVLADDN-UHFFFAOYSA-N 4-(3,4-Methylenedioxyphenyl)-2-butanone Chemical compound CC(=O)CCC1=CC=C2OCOC2=C1 TZJLGGWGVLADDN-UHFFFAOYSA-N 0.000 claims description 3
- RMGXZNGYOADMCM-UHFFFAOYSA-N 4-(3-methyl-4-phenylbut-3-enyl)phenol Chemical compound C=1C=CC=CC=1C=C(C)CCC1=CC=C(O)C=C1 RMGXZNGYOADMCM-UHFFFAOYSA-N 0.000 claims description 3
- VESJWQHRSCMIBZ-UHFFFAOYSA-N 4-(3-methyl-5-phenylpent-3-enyl)phenol Chemical compound C=1C=CC=CC=1CC=C(C)CCC1=CC=C(O)C=C1 VESJWQHRSCMIBZ-UHFFFAOYSA-N 0.000 claims description 3
- XBZCSTFFBHIBLJ-UHFFFAOYSA-N 4-(6-methylheptan-2-yloxy)butanal Chemical compound CC(C)CCCC(C)OCCCC=O XBZCSTFFBHIBLJ-UHFFFAOYSA-N 0.000 claims description 3
- SJYZBTYVRWQFHC-UHFFFAOYSA-N 4-[3-methyl-4-(3-methylphenyl)but-3-enyl]phenol Chemical compound C=1C=CC(C)=CC=1C=C(C)CCC1=CC=C(O)C=C1 SJYZBTYVRWQFHC-UHFFFAOYSA-N 0.000 claims description 3
- GBVCLBDMXNDNPQ-UHFFFAOYSA-N 4-[4-(2-methylbutan-2-yl)cyclohexyl]but-2-enylbenzene Chemical compound C1CC(C(C)(C)CC)CCC1CC=CCC1=CC=CC=C1 GBVCLBDMXNDNPQ-UHFFFAOYSA-N 0.000 claims description 3
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 3
- NICBGBURNHAUSX-UHFFFAOYSA-N 4-methyltridec-2-enylbenzene Chemical compound CCCCCCCCCC(C)C=CCC1=CC=CC=C1 NICBGBURNHAUSX-UHFFFAOYSA-N 0.000 claims description 3
- VEECHONXFDSHGR-UHFFFAOYSA-N 5,7,7-trimethyloct-2-enylbenzene Chemical compound CC(C)(C)CC(C)CC=CCC1=CC=CC=C1 VEECHONXFDSHGR-UHFFFAOYSA-N 0.000 claims description 3
- WNUJDNKMKRZHRZ-UHFFFAOYSA-N 5-(3-methyl-5-phenylpent-3-enyl)-1,3-benzodioxole Chemical compound C=1C=C2OCOC2=CC=1CCC(C)=CCC1=CC=CC=C1 WNUJDNKMKRZHRZ-UHFFFAOYSA-N 0.000 claims description 3
- FLLWRUJVCANHBH-UHFFFAOYSA-N 5-[3-(4-methylphenyl)prop-1-enyl]-1,3-benzodioxole Chemical compound C1=CC(C)=CC=C1CC=CC1=CC=C(OCO2)C2=C1 FLLWRUJVCANHBH-UHFFFAOYSA-N 0.000 claims description 3
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- 101150113676 chr1 gene Proteins 0.000 description 1
- 229930003633 citronellal Natural products 0.000 description 1
- 235000000983 citronellal Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000005595 deprotonation Effects 0.000 description 1
- 238000010537 deprotonation reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- GXANMBISFKBPEX-UHFFFAOYSA-N hex-3c-enal Natural products CCC=CCC=O GXANMBISFKBPEX-UHFFFAOYSA-N 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical class 0.000 description 1
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000007248 oxidative elimination reaction Methods 0.000 description 1
- IPNPIHIZVLFAFP-UHFFFAOYSA-N phosphorus tribromide Chemical compound BrP(Br)Br IPNPIHIZVLFAFP-UHFFFAOYSA-N 0.000 description 1
- ZRLVQFQTCMUIRM-UHFFFAOYSA-N potassium;2-methylbutan-2-olate Chemical compound [K+].CCC(C)(C)[O-] ZRLVQFQTCMUIRM-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- XHTFORWSBVCZQP-UHFFFAOYSA-N tert-butyl-[4-[4-(4-methoxyphenyl)-3-methylbut-3-enyl]phenoxy]-dimethylsilane Chemical compound C1=CC(OC)=CC=C1C=C(C)CCC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1 XHTFORWSBVCZQP-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- UZFLPKAIBPNNCA-FPLPWBNLSA-N α-ionone Chemical compound CC(=O)\C=C/C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-FPLPWBNLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/40—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
- C07C15/42—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals monocyclic
- C07C15/44—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals monocyclic the hydrocarbon substituent containing a carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/40—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
- C07C15/50—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic non-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/40—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
- C07C15/56—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic condensed
- C07C15/58—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic condensed containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/215—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/54—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0003—Compounds of unspecified constitution defined by the chemical reaction for their preparation
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
- C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms
- C11B9/0053—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms both rings being six-membered
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/507—Compounds releasing perfumes by thermal or chemical activation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1021864.2 | 2010-12-23 | ||
| GBGB1021864.2A GB201021864D0 (en) | 2010-12-23 | 2010-12-23 | Organic compounds |
| PCT/EP2011/074003 WO2012085287A1 (en) | 2010-12-23 | 2011-12-23 | Compounds capable of releasing fragrant compounds |
Publications (2)
| Publication Number | Publication Date |
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| BR112013016191A2 BR112013016191A2 (pt) | 2020-08-04 |
| BR112013016191B1 true BR112013016191B1 (pt) | 2021-02-09 |
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| Application Number | Title | Priority Date | Filing Date |
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| BR112013016191-4A BR112013016191B1 (pt) | 2010-12-23 | 2011-12-23 | compostos com capacidade de liberar compostos de fragrância, seu uso, método de geração por oxidação ao ar espontânea de um composto de carbonila e produto de consumo |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9193935B2 (https=) |
| EP (1) | EP2655307B1 (https=) |
| JP (1) | JP6232289B2 (https=) |
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| BR (1) | BR112013016191B1 (https=) |
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| GB (1) | GB201021864D0 (https=) |
| MX (1) | MX341306B (https=) |
| SG (1) | SG190848A1 (https=) |
| WO (1) | WO2012085287A1 (https=) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9718753B2 (en) * | 2013-05-08 | 2017-08-01 | Firmenich Sa | Pro-fragrance compounds |
| WO2014180782A1 (en) * | 2013-05-08 | 2014-11-13 | Firmenich Sa | Pro-fragrance compounds |
| WO2016074698A1 (en) | 2014-11-10 | 2016-05-19 | Givaudan Sa | Improvements in or relating to organic compounds |
| WO2016074699A1 (en) * | 2014-11-10 | 2016-05-19 | Givaudan Sa | Improvments in or relating to organic compounds |
| KR101609323B1 (ko) * | 2015-03-06 | 2016-04-05 | 충북대학교 산학협력단 | 2-메톡시-4-(3-(4-메톡시페닐)프로필-1-엔-1-일)페놀 및 이의 제조방법 |
| GB201703706D0 (en) * | 2017-03-08 | 2017-04-19 | Givaudan Sa | Improvements in or relating to organic compounds |
| EP3533786A1 (en) | 2018-03-02 | 2019-09-04 | Givaudan SA | Thioether precursors for fragrant ketones and aldehydes |
| MX2020009659A (es) * | 2018-06-22 | 2020-10-08 | Firmenich & Cie | Properfume de eter enol. |
| GB201817785D0 (en) | 2018-10-31 | 2018-12-19 | Givaudan Sa | Organic compounds |
| SG11202105724TA (en) | 2018-12-17 | 2021-07-29 | Givaudan Sa | A method of countering malodour in a washing machine comprising the addition of a fragrance precursor |
| US12024692B2 (en) | 2018-12-17 | 2024-07-02 | Givaudan Sa | Method of extending the olfactory effect of a fragrance accord comprising 4-(dodecylthio)-4-methylpentan-2-one |
| EP3823951A1 (en) * | 2018-12-20 | 2021-05-26 | Firmenich SA | Alkyl enol ether properfume |
| CN114502704A (zh) * | 2019-12-03 | 2022-05-13 | 弗门尼舍有限公司 | 烯醇醚香料前体 |
| CN115768740A (zh) * | 2020-07-24 | 2023-03-07 | 弗门尼舍有限公司 | 制备茚丙烯醛衍生物的方法 |
| WO2022261956A1 (en) * | 2021-06-18 | 2022-12-22 | Givaudan Sa | Fragrance compounds |
| WO2023065200A1 (en) | 2021-10-21 | 2023-04-27 | Givaudan Sa | Organic compounds |
| WO2023065203A1 (en) | 2021-10-21 | 2023-04-27 | Givaudan Sa | Organic compounds |
| CN120936587A (zh) | 2023-03-30 | 2025-11-11 | 奇华顿股份有限公司 | 不饱和醚香料前体 |
| WO2025003204A1 (en) | 2023-06-27 | 2025-01-02 | Givaudan Sa | Organic compounds and their use for generating a fragrant alcohol |
| GB202405427D0 (en) | 2024-04-18 | 2024-06-05 | Givaudan Sa | Process |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3115530A (en) | 1960-05-13 | 1963-12-24 | Exxon Research Engineering Co | Preferred alkyl aryl sulfonate detergents |
| CH411836A (de) | 1961-09-07 | 1966-04-30 | Basf Ag | Verfahren zur Herstellung von Mischoligomeren aus 1,3-Dienen und Verbindungen mit aktivierter olefinischer Doppelbindung |
| US3196174A (en) | 1962-03-01 | 1965-07-20 | Exxon Research Engineering Co | Perhydro bis-(isoprenyl) alkyl aryl sulfonates |
| DE2301438A1 (de) | 1973-01-12 | 1974-07-25 | Hoechst Ag | Verwendung von butadienderivaten als optische aufheller fuer waschmittel |
| FR2729661B1 (fr) * | 1995-01-19 | 1997-04-04 | Mane Fils V | Procede de preparation de substances aromatiques par voie biochimique |
| JP3792450B2 (ja) * | 1999-09-03 | 2006-07-05 | 花王株式会社 | 機能性物質放出体 |
| JP3840868B2 (ja) | 2000-02-22 | 2006-11-01 | 株式会社ツムラ | 新規な補骨脂の使用方法 |
| EP1262473A1 (en) * | 2001-05-30 | 2002-12-04 | Givaudan SA | Precursors for fragrant ketones and fragrant aldehydes |
| JP2008303159A (ja) * | 2007-06-06 | 2008-12-18 | Osaka Prefecture Univ | カルボニル化合物の製造方法 |
| GB0717485D0 (en) | 2007-09-08 | 2007-10-17 | Unilever Plc | Improvements relating to fabric conditioners |
| WO2010029462A1 (en) * | 2008-09-12 | 2010-03-18 | Firmenich Sa | Divinyl ether derivatives capable of releasing active aldehydes and ketones and methods of use for perfuming surfaces |
| US8669385B2 (en) * | 2009-10-13 | 2014-03-11 | University Of Central Florida Research Foundation, Inc. | Oxidative cleavage of unsaturated carboxylic acids |
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2010
- 2010-12-23 GB GBGB1021864.2A patent/GB201021864D0/en not_active Ceased
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- 2011-12-23 CN CN201180061738.3A patent/CN103261139B/zh active Active
- 2011-12-23 US US13/996,158 patent/US9193935B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| GB201021864D0 (en) | 2011-02-02 |
| MX2013006034A (es) | 2013-07-03 |
| CN103261139A (zh) | 2013-08-21 |
| US9193935B2 (en) | 2015-11-24 |
| EP2655307A1 (en) | 2013-10-30 |
| MX341306B (es) | 2016-08-15 |
| US20130316938A1 (en) | 2013-11-28 |
| SG190848A1 (en) | 2013-07-31 |
| CN103261139B (zh) | 2015-09-23 |
| EP2655307B1 (en) | 2018-08-01 |
| JP6232289B2 (ja) | 2017-11-15 |
| WO2012085287A1 (en) | 2012-06-28 |
| BR112013016191A2 (pt) | 2020-08-04 |
| JP2014508121A (ja) | 2014-04-03 |
| ES2692179T3 (es) | 2018-11-30 |
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