DE273850C - - Google Patents
Info
- Publication number
- DE273850C DE273850C DENDAT273850D DE273850DA DE273850C DE 273850 C DE273850 C DE 273850C DE NDAT273850 D DENDAT273850 D DE NDAT273850D DE 273850D A DE273850D A DE 273850DA DE 273850 C DE273850 C DE 273850C
- Authority
- DE
- Germany
- Prior art keywords
- ester
- parts
- boiling point
- bromine
- pressure
- 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
- -1 bromodiethylacetylbornyl ester Chemical class 0.000 claims description 9
- 150000002148 esters Chemical group 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000000047 product Substances 0.000 claims description 5
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 229940041616 menthol Drugs 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 125000002298 terpene group Chemical group 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- BDNKAUXMHAPADE-UHFFFAOYSA-N 2-bromo-2-ethylbutanoyl chloride Chemical compound CCC(Br)(CC)C(Cl)=O BDNKAUXMHAPADE-UHFFFAOYSA-N 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims 5
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 4
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims 2
- 238000005406 washing Methods 0.000 claims 2
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 claims 1
- IBTXCRWWEYBTON-UHFFFAOYSA-N 2-bromo-2-propylpentanoyl chloride Chemical compound C(CC)C(C(=O)Cl)(Br)CCC IBTXCRWWEYBTON-UHFFFAOYSA-N 0.000 claims 1
- SMUKODJVMQOSAB-UHFFFAOYSA-N 2-ethylbutanoyl chloride Chemical compound CCC(CC)C(Cl)=O SMUKODJVMQOSAB-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 241000779819 Syncarpia glomulifera Species 0.000 claims 1
- 235000011054 acetic acid Nutrition 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 229960005233 cineole Drugs 0.000 claims 1
- 230000009965 odorless effect Effects 0.000 claims 1
- 239000001739 pinus spp. Substances 0.000 claims 1
- 230000009967 tasteless effect Effects 0.000 claims 1
- 229940036248 turpentine Drugs 0.000 claims 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 4
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 2
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 2
- 229940116229 borneol Drugs 0.000 description 2
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 1
- UEBARDWJXBGYEJ-UHFFFAOYSA-N 2-bromo-3-methylbutanoic acid Chemical compound CC(C)C(Br)C(O)=O UEBARDWJXBGYEJ-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 150000003869 acetamides Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000005554 hypnotics and sedatives Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/22—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system
- C07C35/23—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with hydroxy on a condensed ring system having two rings
- C07C35/28—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with hydroxy on a condensed ring system having two rings the condensed ring system containing seven carbon atoms
- C07C35/29—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with hydroxy on a condensed ring system having two rings the condensed ring system containing seven carbon atoms being a (2.2.1) system
- C07C35/30—Borneol; Isoborneol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE273850C true DE273850C (enrdf_load_html_response) |
Family
ID=530269
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT273850D Active DE273850C (enrdf_load_html_response) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE273850C (enrdf_load_html_response) |
-
0
- DE DENDAT273850D patent/DE273850C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0046970B1 (de) | Gewünschtenfalls mit Natriumsulfit umgesetzte Partialester von mehrwertigen Alkoholen, Verfahren zu ihrer Herstellung und ihre Verwendung als hautfreundliche, nicht ionogene und/oder anionenaktive oberflächenaktive Substanzen | |
| DE2102172C3 (de) | Neue Mittel zur Behandlung und Pflege der Haut | |
| CH616842A5 (enrdf_load_html_response) | ||
| DE273850C (enrdf_load_html_response) | ||
| DE3436863A1 (de) | Antiviral aktive adeninderivate, deren verwendung sowie verfahren zu ihrer herstellung | |
| DE2036935A1 (de) | Verfahren zur Herstellung von Isoniazid derivaten | |
| EP0101918A1 (de) | Verwendung von Aryloxobutensäure-Derivaten in kosmetischen Mitteln, sowie neue Aryloxobutensäurederivate | |
| DE2728922B2 (de) | Glycertintri-3,5,5-trimethylhexanoat | |
| DE1214358B (de) | Roentgenkontrastmittel | |
| DE940402C (de) | Verfahren zur Herstellung eines 4-Pregnen-17ª‡, 21-diol-3, 11, 20-trion-esters bzw. dessen Loesungen oder Suspensionen | |
| DE1618536C (enrdf_load_html_response) | ||
| DE414190C (de) | Verfahren zur Darstellung von Zitronensaeuretribenzylester | |
| DE761283C (de) | Verfahren zur Herstellung von Methacrylsaeureestern | |
| DE261028C (enrdf_load_html_response) | ||
| DE600365C (de) | Verfahren zur Herstellung eines wirksamen Praeparates aus Dioxyphenylisatin bzw. dessen Substitutionsprodukten und Derivaten | |
| WO1982004190A1 (en) | Cosmetic compositions with topical application in the treatment of seborrhea | |
| DE194810C (enrdf_load_html_response) | ||
| DE881039C (de) | Verfahren zur Herstellung des Pentaerythrit-dichlorhydrin-monoschwefligsaeureesters | |
| DE585519C (de) | Verfahren zur Darstellung von organischen Wismutverbindungen | |
| DE253756C (enrdf_load_html_response) | ||
| DE283859C (enrdf_load_html_response) | ||
| DE183185C (enrdf_load_html_response) | ||
| DE412821C (de) | Verfahren zur Reinigung von Naphthensaeuren | |
| DE135351C (enrdf_load_html_response) | ||
| DE638003C (de) | Verfahren zur Herstellung von Vinylestern |