BE402535A - - Google Patents
Info
- Publication number
- BE402535A BE402535A BE402535DA BE402535A BE 402535 A BE402535 A BE 402535A BE 402535D A BE402535D A BE 402535DA BE 402535 A BE402535 A BE 402535A
- Authority
- BE
- Belgium
- Prior art keywords
- hormone
- formula
- hydrogenation
- products
- c18h22o2
- Prior art date
Links
- 229940088597 hormone Drugs 0.000 claims description 10
- 239000005556 hormone Substances 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 7
- 238000005984 hydrogenation reaction Methods 0.000 claims description 7
- APLGXMKUJWCEBP-UHFFFAOYSA-N 1-butoxy-4-[(4-methylphenyl)methoxy]benzene Chemical compound C1=CC(OCCCC)=CC=C1OCC1=CC=C(C)C=C1 APLGXMKUJWCEBP-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000005481 linolenic acid group Chemical group 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 2
- YOCUPQPZWBBYIX-UHFFFAOYSA-N copper nickel Chemical compound [Ni].[Cu] YOCUPQPZWBBYIX-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 229910000570 Cupronickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Landscapes
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE402535A true BE402535A (enrdf_load_html_response) |
Family
ID=68293
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE402535D BE402535A (enrdf_load_html_response) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE402535A (enrdf_load_html_response) |
-
0
- BE BE402535D patent/BE402535A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE10008924A1 (de) | Verfahren zur Herstellung von Phenol | |
| DE69814925T2 (de) | Verfahren zur herstellung von n-propanol | |
| FR2516546A1 (fr) | Procede de recuperation de metaux nobles a partir de residus d'une reaction catalytique de carbonylation | |
| BE402535A (enrdf_load_html_response) | ||
| DE3936252A1 (de) | Reinigung von neopentylglykol | |
| US2096744A (en) | Hydrogenation products of follicle hormones and method of producing same | |
| EP0155610B2 (de) | Verfahren zur Herstellung von 2-Hydroxy-(9H)-carbazol | |
| DE4413176A1 (de) | Verfahren zur Herstellung von Cyclohexyladipaten und Adipinsäure | |
| EP0775693B1 (de) | Verfahren zur Herstellung von 2-Amino-6-chlorphenyl-isopropylsulfan | |
| DE2218316C3 (de) | Verfahren zur Herstellung von Anthrachinon | |
| DD202526A5 (de) | Verfahren zur herstellung von cyclohexanol und/oder cyclohexanon | |
| EP0866052B1 (de) | Verfahren zur Herstellung von 1-Amino-1-methyl-3(4)-amino-methylcyclohexan | |
| DE2504981B2 (de) | Verfahren zur herstellung von propylenoxid und/oder allylalkohol und/oder propionaldehyd und/oder aceton | |
| DE2425653A1 (de) | Verfahren zur herstellung von butandiol | |
| DE2506801A1 (de) | Verfahren zur herstellung von aethylphenolen | |
| SU259856A1 (ru) | Способ получения 1,2,3-циклодедекантриола | |
| BE825563A (fr) | Procede de production d'ethylphenol | |
| KR830001918B1 (ko) | 싸이크로헥사논의 제조방법 | |
| EP0150290A1 (de) | Verfahren zur Herstellung von 13-Oxabicyclo [10.3.0]-pentadecan | |
| JPH059147A (ja) | シクロドデカノンの製造方法 | |
| BE568411A (enrdf_load_html_response) | ||
| DE2003915A1 (de) | Verfahren zur Herstellung von 1-Phenylnaphthalin und 1-Phenyl-4-[1'-phenyl-aethyl-(1')]-naphthalin | |
| DE3628357A1 (de) | Verfahren zur behandlung von waessrigen loesungen, die bei der carboxyalkylierung von olefinisch ungesaettigten verbindungen anfallen | |
| DE1933538A1 (de) | Verfahren zur Herstellung von Allylalkohol | |
| BE454955A (enrdf_load_html_response) |