HU222273B1 - Eljárás savkloridok előállítására savak és/vagy anhidridek nyomás alatt végzett foszgénezésével - Google Patents
Eljárás savkloridok előállítására savak és/vagy anhidridek nyomás alatt végzett foszgénezésével Download PDFInfo
- Publication number
- HU222273B1 HU222273B1 HU9700535A HUP9700535A HU222273B1 HU 222273 B1 HU222273 B1 HU 222273B1 HU 9700535 A HU9700535 A HU 9700535A HU P9700535 A HUP9700535 A HU P9700535A HU 222273 B1 HU222273 B1 HU 222273B1
- Authority
- HU
- Hungary
- Prior art keywords
- substituted
- acid
- unsubstituted
- aryl
- reaction
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims abstract description 51
- 238000000034 method Methods 0.000 title claims abstract description 40
- 150000008064 anhydrides Chemical class 0.000 title claims abstract description 25
- 150000007513 acids Chemical class 0.000 title claims description 6
- 150000001805 chlorine compounds Chemical class 0.000 title description 5
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000003054 catalyst Substances 0.000 claims abstract description 31
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 7
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 6
- 150000002763 monocarboxylic acids Chemical class 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 41
- 125000003118 aryl group Chemical group 0.000 claims description 29
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 15
- 125000004104 aryloxy group Chemical group 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 125000005110 aryl thio group Chemical group 0.000 claims description 12
- 125000001188 haloalkyl group Chemical group 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 238000007872 degassing Methods 0.000 claims description 5
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 5
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims description 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000002837 carbocyclic group Chemical group 0.000 claims description 3
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 abstract description 7
- 238000000926 separation method Methods 0.000 abstract description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 19
- 238000012360 testing method Methods 0.000 description 14
- 239000012429 reaction media Substances 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 8
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- 235000021355 Stearic acid Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 7
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 7
- 239000008117 stearic acid Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 6
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- PGZVFRAEAAXREB-UHFFFAOYSA-N 2,2-dimethylpropanoyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC(=O)C(C)(C)C PGZVFRAEAAXREB-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000005711 Benzoic acid Substances 0.000 description 4
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 4
- UHOVQNZJYSORNB-MZWXYZOWSA-N benzene-d6 Chemical compound [2H]C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H] UHOVQNZJYSORNB-MZWXYZOWSA-N 0.000 description 4
- 235000010233 benzoic acid Nutrition 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 4
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 4
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- JVSFQJZRHXAUGT-UHFFFAOYSA-N 2,2-dimethylpropanoyl chloride Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- -1 dicarboxylic acid chlorides Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000004995 haloalkylthio group Chemical group 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- JUJWROOIHBZHMG-RALIUCGRSA-N pyridine-d5 Chemical compound [2H]C1=NC([2H])=C([2H])C([2H])=C1[2H] JUJWROOIHBZHMG-RALIUCGRSA-N 0.000 description 2
- 229910052594 sapphire Inorganic materials 0.000 description 2
- 239000010980 sapphire Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- RPAJSBKBKSSMLJ-DFWYDOINSA-N (2s)-2-aminopentanedioic acid;hydrochloride Chemical class Cl.OC(=O)[C@@H](N)CCC(O)=O RPAJSBKBKSSMLJ-DFWYDOINSA-N 0.000 description 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 1
- MLQBTMWHIOYKKC-KTKRTIGZSA-N (z)-octadec-9-enoyl chloride Chemical compound CCCCCCCC\C=C/CCCCCCCC(Cl)=O MLQBTMWHIOYKKC-KTKRTIGZSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- WFSGQBNCVASPMW-UHFFFAOYSA-N 2-ethylhexanoyl chloride Chemical compound CCCCC(CC)C(Cl)=O WFSGQBNCVASPMW-UHFFFAOYSA-N 0.000 description 1
- OFTKFKYVSBNYEC-UHFFFAOYSA-N 2-furoyl chloride Chemical compound ClC(=O)C1=CC=CO1 OFTKFKYVSBNYEC-UHFFFAOYSA-N 0.000 description 1
- GPZXFICWCMCQPF-UHFFFAOYSA-N 2-methylbenzoyl chloride Chemical compound CC1=CC=CC=C1C(Cl)=O GPZXFICWCMCQPF-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- WPYMKLBDIGXBTP-CDYZYAPPSA-N benzene(13C)carboxylic acid Chemical compound O[13C](=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-CDYZYAPPSA-N 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- MVPPADPHJFYWMZ-IDEBNGHGSA-N chlorobenzene Chemical group Cl[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 MVPPADPHJFYWMZ-IDEBNGHGSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000012812 general test Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- REEZZSHJLXOIHL-UHFFFAOYSA-N octanoyl chloride Chemical compound CCCCCCCC(Cl)=O REEZZSHJLXOIHL-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- PNQBEPDZQUOCNY-UHFFFAOYSA-N trifluoroacetyl chloride Chemical compound FC(F)(F)C(Cl)=O PNQBEPDZQUOCNY-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9602795A FR2745567B1 (fr) | 1996-02-29 | 1996-02-29 | Phosgenation sous pression des acides pour la prodution des chlorures d'acides |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| HU9700535D0 HU9700535D0 (en) | 1997-04-28 |
| HUP9700535A2 HUP9700535A2 (hu) | 1998-06-29 |
| HUP9700535A3 HUP9700535A3 (en) | 1999-06-28 |
| HU222273B1 true HU222273B1 (hu) | 2003-05-28 |
Family
ID=9489904
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU9700535A HU222273B1 (hu) | 1996-02-29 | 1997-02-28 | Eljárás savkloridok előállítására savak és/vagy anhidridek nyomás alatt végzett foszgénezésével |
Country Status (9)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007108046A (ja) * | 2005-10-14 | 2007-04-26 | Idemitsu Kosan Co Ltd | 二層分離温度測定装置およびその測定方法 |
| RU2456275C2 (ru) * | 2008-03-18 | 2012-07-20 | Мицуй Кемикалс Агро, ИНК | Способ получения фторсодержащего производного ацилуксусной кислоты, способ получения фторсодержащего производного сложного эфира пиразолкарбоновой кислоты и способ получения фторсодержащего производного пиразолкарбоновой кислоты |
| CN104072347B (zh) * | 2014-06-30 | 2016-07-13 | 湖南海利化工股份有限公司 | 4-烷氧基-1，1，1-三氟-3-丁烯-2-酮的制备方法 |
| CN105384640B (zh) * | 2015-10-26 | 2017-07-04 | 安徽广信农化股份有限公司 | 一种对硝基苯甲酰氯的尾气处理工艺 |
| CN105254505A (zh) * | 2015-10-26 | 2016-01-20 | 安徽广信农化股份有限公司 | 一种对硝基苯甲酰氯的精制工艺 |
| CN105384641A (zh) * | 2015-10-26 | 2016-03-09 | 安徽广信农化股份有限公司 | 一种对硝基苯甲酰氯的废水处理工艺 |
| CN105524017B (zh) * | 2015-12-24 | 2017-06-30 | 江苏瀚联生物科技有限公司 | 2‑甲基氨基‑5‑叔丁基‑1，3，4‑噻二唑的制备方法 |
| CN105585478A (zh) * | 2016-03-08 | 2016-05-18 | 天津市敬业精细化工有限公司 | 一种酰氯的制备方法 |
| CN106674166B (zh) * | 2016-12-20 | 2018-09-25 | 重庆市化工研究院 | 呋喃甲酰氯的制备方法 |
| CN113402383A (zh) * | 2020-03-17 | 2021-09-17 | 上海祖玥新材料科技有限公司 | 一种2-乙基己酸与光气反应合成2-乙基己酰氯的方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB402328A (en) * | 1932-04-29 | 1933-11-30 | Ig Farbenindustrie Ag | Improvements in the manufacture of acetyl-chloride |
| NL175521C (nl) * | 1973-04-26 | 1984-11-16 | Hoechst Ag | Werkwijze voor het bereiden van carbonzuurchloriden. |
| FR2232532A1 (en) * | 1973-06-05 | 1975-01-03 | Poudres & Explosifs Ste Nale | Gas phase acid chloride prodn. - from acid and phosgene in presence of active carbon catalyst |
| DE3535984A1 (de) * | 1985-10-09 | 1987-04-09 | Bayer Ag | Verfahren zur herstellung von aromatischen carbonsaeurechloriden |
| DE4129822A1 (de) * | 1991-09-07 | 1993-03-11 | Basf Ag | Verfahren zur herstellung von carbonsaeurehalogeniden |
-
1996
- 1996-02-29 FR FR9602795A patent/FR2745567B1/fr not_active Expired - Fee Related
-
1997
- 1997-02-20 IL IL12027297A patent/IL120272A0/xx unknown
- 1997-02-24 DE DE19707285A patent/DE19707285A1/de not_active Withdrawn
- 1997-02-25 FR FR9702461A patent/FR2745568B1/fr not_active Expired - Fee Related
- 1997-02-25 KR KR1019970005815A patent/KR100599065B1/ko not_active Expired - Fee Related
- 1997-02-27 GB GB9704047A patent/GB2310661B/en not_active Expired - Fee Related
- 1997-02-27 JP JP9044230A patent/JPH09323953A/ja active Pending
- 1997-02-28 HU HU9700535A patent/HU222273B1/hu not_active IP Right Cessation
- 1997-02-28 BR BR9700326A patent/BR9700326A/pt not_active IP Right Cessation
- 1997-02-28 CN CN97104714A patent/CN1071303C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| FR2745567A1 (fr) | 1997-09-05 |
| GB9704047D0 (en) | 1997-04-16 |
| CN1163881A (zh) | 1997-11-05 |
| HUP9700535A3 (en) | 1999-06-28 |
| BR9700326A (pt) | 1998-10-27 |
| CN1071303C (zh) | 2001-09-19 |
| IL120272A0 (en) | 1997-06-10 |
| JPH09323953A (ja) | 1997-12-16 |
| FR2745568B1 (fr) | 1998-08-21 |
| KR100599065B1 (ko) | 2006-12-05 |
| FR2745568A1 (fr) | 1997-09-05 |
| GB2310661B (en) | 1998-12-02 |
| DE19707285A1 (de) | 1997-09-04 |
| HU9700535D0 (en) | 1997-04-28 |
| HUP9700535A2 (hu) | 1998-06-29 |
| FR2745567B1 (fr) | 1998-04-10 |
| GB2310661A (en) | 1997-09-03 |
| KR970061845A (ko) | 1997-09-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101982952B1 (ko) | 피라졸 유도체의 제조 방법 | |
| EP0064986B1 (en) | Preparation of acetic anhydride | |
| KR100228408B1 (ko) | 지방족 폴리이소시아네이트의 제조방법 | |
| HU222273B1 (hu) | Eljárás savkloridok előállítására savak és/vagy anhidridek nyomás alatt végzett foszgénezésével | |
| JPH02266A (ja) | トリフルオロメタンスルホニルクロリドの製造方法 | |
| KR102720359B1 (ko) | 공기 산화에 의한 3-메틸-2-니트로벤조산의 제조 공정 | |
| US2657233A (en) | Process of preparing dicarboxylic acid chlorides | |
| JP2001514240A (ja) | クロロホルメートを製造するためのアルコールの加圧下でのホスゲン化 | |
| JP3907219B2 (ja) | ｏ−クロロメチル安息香酸クロリドの製造方法 | |
| US6002043A (en) | Phosgenation under pressure of acids and of anhydrides of acid chlorides | |
| US5258530A (en) | Process for producing biphenyltetracarboxylic dianhydride | |
| JP4292387B2 (ja) | ビフェニルテトラカルボン酸テトラエステルの製造方法 | |
| KR20010052528A (ko) | 알킬 클로라이드, 알케닐 클로라이드 및 알키닐클로라이드의 제조 방법 | |
| WO2011037929A2 (en) | Pd(ii)-catalyzed hydroxylation of arenes with o2 or air | |
| KR100584631B1 (ko) | 히드라진 히드레이트의 제조방법 | |
| JPS60255752A (ja) | ２‐クロルプロピオン酸エステルの製造法 | |
| RU2838764C1 (ru) | Способ получения хлорангидрида 2,4-дихлор-2-дихлорфосфорилбутановой кислоты | |
| US3931241A (en) | Method for preparation of citraconic acid and derivatives thereof | |
| JPH01261344A (ja) | ２，２，６，６‐テトラクロロシクロヘキサノンの製造法 | |
| JP4238348B2 (ja) | ラクタム製造法 | |
| KR101399916B1 (ko) | 카복실산 클로라이드 화합물의 제조방법 | |
| WO2008033335A2 (en) | Process for preparing fluorinated carboxylic acids | |
| US3458573A (en) | Preparation of monochloroacetoacetamides | |
| KR820001078B1 (ko) | 알파-클로로-디에틸카르보네이트의 제조방법 | |
| CN118786113A (zh) | 联菲化合物或其碱金属盐 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HFG4 | Patent granted, date of granting |
Effective date: 20030314 |
|
| MM4A | Lapse of definitive patent protection due to non-payment of fees |