DE153924C - - Google Patents
Info
- Publication number
- DE153924C DE153924C DE1901153924D DE153924DA DE153924C DE 153924 C DE153924 C DE 153924C DE 1901153924 D DE1901153924 D DE 1901153924D DE 153924D A DE153924D A DE 153924DA DE 153924 C DE153924 C DE 153924C
- Authority
- DE
- Germany
- Prior art keywords
- chlorohydrate
- pinene
- camphene
- free
- chlorine
- 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.)
- Expired - Lifetime
Links
- GRWFGVWFFZKLTI-UHFFFAOYSA-N (+-)-2-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims description 12
- CRPUJAZIXJMDBK-DTWKUNHWSA-N (+)-camphene Chemical compound C1C[C@@H]2C(=C)C(C)(C)[C@H]1C2 CRPUJAZIXJMDBK-DTWKUNHWSA-N 0.000 claims description 9
- 229930006739 camphene Natural products 0.000 claims description 9
- 239000000344 soap Substances 0.000 claims description 8
- 239000002585 base Substances 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 150000001447 alkali salts Chemical class 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 2
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 2
- WFXRJNDIBXZNJK-KVVVOXFISA-N azanium;(Z)-octadec-9-enoate Chemical compound N.CCCCCCCC\C=C/CCCCCCCC(O)=O WFXRJNDIBXZNJK-KVVVOXFISA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- XXZAOMJCZBZKPV-UHFFFAOYSA-N 3-chloro-4,7,7-trimethylbicyclo[2.2.1]heptane Chemical compound C1CC2(C)C(Cl)CC1C2(C)C XXZAOMJCZBZKPV-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 230000001476 alcoholic Effects 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT19308D AT19308B (pt) | 1901-11-09 | 1903-03-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE153924C true DE153924C (pt) |
Family
ID=420511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1901153924D Expired - Lifetime DE153924C (pt) | 1901-11-09 | 1901-11-09 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE153924C (pt) |
-
1901
- 1901-11-09 DE DE1901153924D patent/DE153924C/de not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1059459B (de) | Verfahren zur Herstellung des therapeutisch wertvollen 3-Sulfanilamido-5-methylisoxazols | |
| DE153924C (pt) | ||
| DE2447824A1 (de) | Herstellung von c tief 1 -c tief 7 aliphatischen hydrocarbylestern von n- eckige klammer auf 2,6-di(c tief 1 -c tief 7 -alkyl)phenyl eckige klammer zu alpha-aminocarbonsaeuren | |
| DE1301312B (de) | Verfahren zur Herstellung von Pyrryl-(2)-acetonitrilen | |
| DE156901C (pt) | ||
| DE2725780C2 (pt) | ||
| DE866193C (de) | Verfahren zur Herstellung von in der Amidgruppe substituierten Carbonsaeureamiden | |
| DE213713C (pt) | ||
| DE202696C (pt) | ||
| DE708349C (de) | Verfahren zur Herstellung saeureamidartiger Kondensationsprodukte | |
| DE489845C (de) | Verfahren zur Darstellung von N-Arylsulfoderivaten primaerer und sekundaerer Amine | |
| DE515540C (de) | Verfahren zur Darstellung von Diacidylderivaten des meta-Xylols | |
| DE126311C (pt) | ||
| DE878943C (de) | Verfahren zur Herstellung ungesaettigter Nitrile | |
| DE741891C (de) | Verfahren zur Herstellung wasserloeslicher stickstoffhaltiger Kondensationsprodukte | |
| DE281097C (pt) | ||
| DE1237560B (de) | Verfahren zur Herstellung von Cyanameisensaeurethiolestern | |
| DE226228C (pt) | ||
| DE765787C (de) | Verfahren zur Herstellung von Umsetzungsprodukten von Formaldehyd mit Blausaeure | |
| DE631462C (de) | Verfahren zur Herstellung von Monomethyl-p-aminophenolsulfat | |
| DE1073501B (de) | Verfahren zur Herstellung von am Stick stoffatom durch eine aliphatische cyclo ahphatische oder aliphatisch aromatische Gruppe substituierten ß Ammobuttersau ren bzw deren Salzen | |
| DE213155C (pt) | ||
| DE737572C (de) | Verfahren zur Herstellung von Dihydrofollikelhormonen | |
| DE591821C (de) | Herstellung von Chinonen neben Chromchlorid | |
| DE338281C (de) | Verfahren zur Herstellung von Alkylaethern des Vinylalkohols und seiner Homologen |