DE99057C - - Google Patents
Info
- Publication number
- DE99057C DE99057C DENDAT99057D DE99057DA DE99057C DE 99057 C DE99057 C DE 99057C DE NDAT99057 D DENDAT99057 D DE NDAT99057D DE 99057D A DE99057D A DE 99057DA DE 99057 C DE99057 C DE 99057C
- Authority
- DE
- Germany
- Prior art keywords
- phenol
- carbonate
- guaiacol
- phenols
- carbonates
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 14
- YGYAWVDWMABLBF-UHFFFAOYSA-N phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 150000002989 phenols Chemical class 0.000 claims description 5
- AOGYCOYQMAVAFD-UHFFFAOYSA-N Chloroformic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N Guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 14
- 229960001867 Guaiacol Drugs 0.000 description 7
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 6
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 6
- 229960004873 LEVOMENTHOL Drugs 0.000 description 6
- 229940041616 Menthol Drugs 0.000 description 6
- CQDGTJPVBWZJAZ-UHFFFAOYSA-M ethyl carbonate Chemical compound CCOC([O-])=O CQDGTJPVBWZJAZ-UHFFFAOYSA-M 0.000 description 5
- -1 phenols chlorocarbonic acid esters Chemical class 0.000 description 5
- ROORDVPLFPIABK-UHFFFAOYSA-N Diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000004651 carbonic acid esters Chemical class 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- UCRUTNJGISGZMY-UHFFFAOYSA-N 2-(hydroxymethyl)-3-methyl-6-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)C1CCC(C)C(CO)C1O UCRUTNJGISGZMY-UHFFFAOYSA-N 0.000 description 1
- 210000002588 AT2 Anatomy 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N Ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- 241000207923 Lamiaceae Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ORUJFMPWKPVXLZ-UHFFFAOYSA-N bis(2-methoxyphenyl) carbonate Chemical compound COC1=CC=CC=C1OC(=O)OC1=CC=CC=C1OC ORUJFMPWKPVXLZ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- OFDKFNZHXJWFNS-UHFFFAOYSA-N ethyl (2-methoxyphenyl) carbonate Chemical compound CCOC(=O)OC1=CC=CC=C1OC OFDKFNZHXJWFNS-UHFFFAOYSA-N 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 229950010370 guaiacol carbonate Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- QIIPQYDSKRYMFG-UHFFFAOYSA-M phenyl carbonate Chemical class [O-]C(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-M 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/02—Preparation of esters of carbonic or haloformic acids from phosgene or haloformates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE99057C true DE99057C (ja) |
Family
ID=369966
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT99057D Active DE99057C (ja) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE99057C (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009123355A2 (en) * | 2008-04-01 | 2009-10-08 | Takasago International Corporation | Cooling sensation agent composition and sensory stimulation agent composition |
-
0
- DE DENDAT99057D patent/DE99057C/de active Active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009123355A2 (en) * | 2008-04-01 | 2009-10-08 | Takasago International Corporation | Cooling sensation agent composition and sensory stimulation agent composition |
WO2009123355A3 (en) * | 2008-04-01 | 2009-12-10 | Takasago International Corporation | Cooling sensation agent composition and sensory stimulation agent composition |
US8632792B2 (en) | 2008-04-01 | 2014-01-21 | Takasago International Corporation | Cooling sensation agent composition and sensory stimulation agent composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1493920A1 (de) | Aminoaether und Verfahren zu deren Herstellung | |
DE99057C (ja) | ||
DE1495397C3 (de) | Verfahren zur Herstellung von hochmolekularen Polyestern der Kohlensäure | |
DE1468920A1 (de) | Verfahren zur Herstellung von neuen Dibenzocycloheptadienderivaten | |
DE1668968A1 (de) | Neue organische Verbindungen | |
DE2312963A1 (de) | Dioxolane | |
DE181175C (ja) | ||
DE730789C (de) | Verfahren zur Darstellung von 1-Oxyaryloxy-3-alkoxy-2-propanolen bzw. -2-propanonen | |
DE1668550C (ja) | ||
DE169787C (ja) | ||
DE254471C (ja) | ||
DE1039063B (de) | Verfahren zur Herstellung eines antipyretisch wirksamen, substituierten 1, 2-Diphenyl-3, 5-dioxo-pyrazolidins und dessen Salzen | |
DE409780C (de) | Verfahren zur Herstellung von N-Mono- und Polycarbonsaeureestern einseitig substituierter Alkylendiamine | |
DE69730615T2 (de) | Verfahren zur herstellung eines tetrahydropyridinderivates | |
DE957036C (de) | Verfahren zur Herstellung von neuen, den Muskeltonus beeinflussenden Diammoniumverbindungen | |
DE2936416C2 (ja) | ||
DE1643492B2 (de) | 1,3,5-trithiacyclohexane und deren herstellung | |
DE822386C (de) | Verfahren zur Herstellung von Dialkyloxybenzoesaeuredialkylaminoalkylamiden | |
DE272337C (ja) | ||
DE134308C (ja) | ||
DE1493912C (de) | 2-(Naphthyl-l)-3-furyl-beziehungsweise -3-tetrahydrofuryl-propionsäure und deren Natriumsalze sowie Verfahren zu deren Herstellung | |
DE186111C (ja) | ||
DE881039C (de) | Verfahren zur Herstellung des Pentaerythrit-dichlorhydrin-monoschwefligsaeureesters | |
DE550403C (de) | Verfahren zur Herstellung von Vinylaethern | |
DE2802519A1 (de) | Neue benzophenonderivate, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammensetzungen |