DE149791C - - Google Patents
Info
- Publication number
- DE149791C DE149791C DENDAT149791D DE149791DA DE149791C DE 149791 C DE149791 C DE 149791C DE NDAT149791 D DENDAT149791 D DE NDAT149791D DE 149791D A DE149791D A DE 149791DA DE 149791 C DE149791 C DE 149791C
- Authority
- DE
- Germany
- Prior art keywords
- pinene
- ammonia
- chlorine
- free
- alcoholic
- 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
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 21
- 229910021529 ammonia Inorganic materials 0.000 claims description 10
- 230000001476 alcoholic effect Effects 0.000 claims description 6
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 3
- 241000723346 Cinnamomum camphora Species 0.000 claims description 3
- 229930008380 camphor Natural products 0.000 claims description 3
- 229960000846 camphor Drugs 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims 1
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 6
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 3
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 3
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 3
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 3
- 229930006739 camphene Natural products 0.000 description 3
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 3
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 229940116229 borneol Drugs 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Natural products CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-MRTMQBJTSA-N Isoborneol Natural products C1C[C@@]2(C)[C@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-MRTMQBJTSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- GVLGAFRNYJVHBC-UHFFFAOYSA-N hydrate;hydrobromide Chemical compound O.Br GVLGAFRNYJVHBC-UHFFFAOYSA-N 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- -1 isobornyl ethyl ether Chemical compound 0.000 description 1
- SHUUILSADJSVGR-UHFFFAOYSA-N molecular iodine hydrate Chemical compound O[H].II SHUUILSADJSVGR-UHFFFAOYSA-N 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
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
- C07C1/30—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms by splitting-off the elements of hydrogen halide from a single molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE149791C true DE149791C (enExample) |
Family
ID=416770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT149791D Active DE149791C (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE149791C (enExample) |
-
0
- DE DENDAT149791D patent/DE149791C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE149791C (enExample) | ||
| DE1543680A1 (de) | Kontinuierliches Verfahren zum Herstellen von Hexamethylendiamin | |
| DE801987C (de) | Verfahren zur Herstellung von Hexachloraethan | |
| DE539177C (de) | Verfahren zur Darstellung von n-Butyraldehyd | |
| DE2704547A1 (de) | Verfahren zur herstellung von dihydromyrcenol | |
| DE704494C (de) | Verfahren zur Herstellung von aliphatischen Carbonsaeurenitrilen | |
| DE249868C (enExample) | ||
| DE234290C (enExample) | ||
| DE881500C (de) | Verfahren zur Herstellung von Di- und Polychloralkylen und ªÏ,ªÏ'-Dichloralkylaethern | |
| DE656838C (de) | Verfahren zur Darstellung von Alanin durch Verseifen von Alaninnitril mit Alkalilauge | |
| DE723498C (de) | Verfahren zur Herstellung von aliphatischen Oxyaldehyden und Oxyketonen | |
| DE821202C (de) | Verfahren zur Herstellung von Butyraldehyd | |
| DE116310C (enExample) | ||
| CH215655A (de) | Verfahren zur Herstellung von Pentachlorbutadien. | |
| DE567118C (de) | Verfahren zur Herstellung von Aceton aus Acetylen | |
| AT120867B (de) | Verfahren zur Darstellung sekundärer Alkohole aus Propylen oder dessen Homologen. | |
| DE1443377A1 (de) | Verfahren zur Herstellung von Cyclohexen bzw. Methylcyclohexen | |
| DE151019C (enExample) | ||
| DE895450C (de) | Verfahren zur Herstellung von Allylalkohol | |
| DE878641C (de) | Verfahren zur Herstellung von hoehermolekularen Aminen | |
| DE863189C (de) | Verfahren zur Herstellung von Butantriol-(1,2,4) | |
| DE721684C (de) | Entkaelkungsmittel | |
| DE864251C (de) | Verfahren zur Herstellung hydroaromatischer Aldehyde und bzw. oder Alkohole | |
| DE532007C (de) | Verfahren zur Herstellung von inaktivem Menthol | |
| DE956046C (de) | Verfahren zur Herstellung von Diphenylamin und kernalkylsubstituierten Diphenylaminen |