DE122096C - - Google Patents
Info
- Publication number
- DE122096C DE122096C DENDAT122096D DE122096DA DE122096C DE 122096 C DE122096 C DE 122096C DE NDAT122096 D DENDAT122096 D DE NDAT122096D DE 122096D A DE122096D A DE 122096DA DE 122096 C DE122096 C DE 122096C
- Authority
- DE
- Germany
- Prior art keywords
- carbinol
- ethyl
- methyl
- acid esters
- secondary alcohols
- 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
- 150000003333 secondary alcohols Chemical class 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 7
- 150000004651 carbonic acid esters Chemical class 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 4
- 229940112021 centrally acting muscle relaxants Carbamic acid esters Drugs 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims 1
- 238000006011 modification reaction Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004432 carbon atoms Chemical group C* 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- DIFOPVYBCNZAIF-UHFFFAOYSA-N ethyl pentan-2-yl carbonate Chemical compound CCCC(C)OC(=O)OCC DIFOPVYBCNZAIF-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- SZNSABMHTKBDFG-UHFFFAOYSA-N methyl pentan-2-yl carbonate Chemical compound CCCC(C)OC(=O)OC SZNSABMHTKBDFG-UHFFFAOYSA-N 0.000 description 2
- -1 methylpropylcarbinol urethane Chemical compound 0.000 description 2
- 230000001264 neutralization Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N 2-Butanol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
- QNVRIHYSUZMSGM-UHFFFAOYSA-N 2-Hexanol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 1
- ISTJMQSHILQAEC-UHFFFAOYSA-N 2-Methyl-3-pentanol Chemical compound CCC(O)C(C)C ISTJMQSHILQAEC-UHFFFAOYSA-N 0.000 description 1
- JYVLIDXNZAXMDK-UHFFFAOYSA-N 2-Pentanol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 1
- ZOCHHNOQQHDWHG-UHFFFAOYSA-N 3-Hexanol Chemical compound CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 0.000 description 1
- MXLMTQWGSQIYOW-UHFFFAOYSA-N 3-Methyl-2-butanol Chemical compound CC(C)C(C)O MXLMTQWGSQIYOW-UHFFFAOYSA-N 0.000 description 1
- AQIXEPGDORPWBJ-UHFFFAOYSA-N 3-Pentanol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 1
- RGCZULIFYUPTAR-UHFFFAOYSA-N 5-methylhexan-3-ol Chemical compound CCC(O)CC(C)C RGCZULIFYUPTAR-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- WFKBZDONIAVHFI-UHFFFAOYSA-N C(O)(=O)OC(CCC)(C)CC Chemical compound C(O)(=O)OC(CCC)(C)CC WFKBZDONIAVHFI-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KMIKGMBRCMHTMM-UHFFFAOYSA-N butan-2-yl ethyl carbonate Chemical compound CCOC(=O)OC(C)CC KMIKGMBRCMHTMM-UHFFFAOYSA-N 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DLPOJRFSTVLOPW-UHFFFAOYSA-N ethyl 2-methylpentan-3-yl carbonate Chemical compound CCOC(=O)OC(CC)C(C)C DLPOJRFSTVLOPW-UHFFFAOYSA-N 0.000 description 1
- XXFPNRVPXCFNCD-UHFFFAOYSA-N ethyl 3-methylbutan-2-yl carbonate Chemical compound CCOC(=O)OC(C)C(C)C XXFPNRVPXCFNCD-UHFFFAOYSA-N 0.000 description 1
- QOZYFCWNYSKZEY-UHFFFAOYSA-N ethyl 5-methylhexan-3-yl carbonate Chemical compound CCOC(=O)OC(CC)CC(C)C QOZYFCWNYSKZEY-UHFFFAOYSA-N 0.000 description 1
- MDVJJGGCAIBYDH-UHFFFAOYSA-N ethyl heptan-4-yl carbonate Chemical compound CCCC(CCC)OC(=O)OCC MDVJJGGCAIBYDH-UHFFFAOYSA-N 0.000 description 1
- CVNLTCBLRAACET-UHFFFAOYSA-N ethyl hexan-2-yl carbonate Chemical compound CCCCC(C)OC(=O)OCC CVNLTCBLRAACET-UHFFFAOYSA-N 0.000 description 1
- YMBUHDUFLDXZMS-UHFFFAOYSA-N ethyl pentan-3-yl carbonate Chemical compound CCOC(=O)OC(CC)CC YMBUHDUFLDXZMS-UHFFFAOYSA-N 0.000 description 1
- YVBCULSIZWMTFY-UHFFFAOYSA-N heptan-4-ol Chemical compound CCCC(O)CCC YVBCULSIZWMTFY-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE122096C true DE122096C (pt) |
Family
ID=391045
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT122096D Active DE122096C (pt) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE122096C (pt) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3621042A (en) * | 1969-03-20 | 1971-11-16 | May F Baker Ltd | Process for the preparation of methyl {11 -aminobenzenesulphonylcarbamate |
| US3933846A (en) * | 1972-06-08 | 1976-01-20 | Bayer Aktiengesellschaft | Preparation of benzimidazol-2-yl-carbamic acid alkyl esters |
-
0
- DE DENDAT122096D patent/DE122096C/de active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3621042A (en) * | 1969-03-20 | 1971-11-16 | May F Baker Ltd | Process for the preparation of methyl {11 -aminobenzenesulphonylcarbamate |
| US3933846A (en) * | 1972-06-08 | 1976-01-20 | Bayer Aktiengesellschaft | Preparation of benzimidazol-2-yl-carbamic acid alkyl esters |
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