DD298107A5 - Verfahren zur herstellung von 3-hydroxy-1,3,5(10)-estratrien-17-on - Google Patents
Verfahren zur herstellung von 3-hydroxy-1,3,5(10)-estratrien-17-on Download PDFInfo
- Publication number
- DD298107A5 DD298107A5 DD90344084A DD34408490A DD298107A5 DD 298107 A5 DD298107 A5 DD 298107A5 DD 90344084 A DD90344084 A DD 90344084A DD 34408490 A DD34408490 A DD 34408490A DD 298107 A5 DD298107 A5 DD 298107A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- pyrolysis
- androstadiene
- dione
- heated
- temperature
- Prior art date
Links
- 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 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- 238000000034 method Methods 0.000 claims abstract description 26
- 238000000197 pyrolysis Methods 0.000 claims abstract description 25
- LUJVUUWNAPIQQI-UHFFFAOYSA-N (+)-androsta-1,4-diene-3,17-dione Natural products O=C1C=CC2(C)C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 LUJVUUWNAPIQQI-UHFFFAOYSA-N 0.000 claims abstract description 17
- LUJVUUWNAPIQQI-QAGGRKNESA-N androsta-1,4-diene-3,17-dione Chemical compound O=C1C=C[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 LUJVUUWNAPIQQI-QAGGRKNESA-N 0.000 claims abstract description 17
- 239000000852 hydrogen donor Substances 0.000 claims abstract 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims description 24
- 238000002360 preparation method Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 11
- 229960003399 estrone Drugs 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 6
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 229920013685 Estron Polymers 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- KCVRVAZIJULBEF-QAGGRKNESA-N (8R,9S,10R,13S,14S)-10,13-dimethyl-7,8,9,11,12,14-hexahydro-6H-cyclopenta[a]phenanthrene-3,17-dione Chemical compound C[C@@]12C(C=C[C@H]1[C@@H]1CCC3=CC(C=C[C@]3(C)[C@H]1CC2)=O)=O KCVRVAZIJULBEF-QAGGRKNESA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0011—Androstane derivatives substituted in position 17 by a keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0051—Estrane derivatives
- C07J1/0059—Estrane derivatives substituted in position 17 by a keto group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3931820A DE3931820A1 (de) | 1989-09-20 | 1989-09-20 | Verfahren zur herstellung von 3-hydroxyl-1,3,5(10)-estratrien-17-on |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD298107A5 true DD298107A5 (de) | 1992-02-06 |
Family
ID=6390056
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD90344084A DD298107A5 (de) | 1989-09-20 | 1990-09-18 | Verfahren zur herstellung von 3-hydroxy-1,3,5(10)-estratrien-17-on |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5151533A (da) |
| EP (1) | EP0445244B1 (da) |
| JP (1) | JP2933713B2 (da) |
| AT (1) | ATE128142T1 (da) |
| CA (1) | CA2042029A1 (da) |
| DD (1) | DD298107A5 (da) |
| DE (2) | DE3931820A1 (da) |
| DK (1) | DK0445244T3 (da) |
| ES (1) | ES2078351T3 (da) |
| WO (1) | WO1991004264A1 (da) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1247566A1 (de) * | 2001-04-02 | 2002-10-09 | Michael Prof. Dr. Buback | Verfahren zur schnellen thermischen Anregung einer chemischen Reaktion in einer überkritisch fluiden Lösung |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5126865A (en) * | 1974-08-22 | 1976-03-05 | Mitsubishi Chem Ind | 33 hidorokishi 199 noru 1*3*5 * 10 * torienkeisuteroidono seizoho |
-
1989
- 1989-09-20 DE DE3931820A patent/DE3931820A1/de not_active Withdrawn
-
1990
- 1990-09-06 CA CA002042029A patent/CA2042029A1/en not_active Abandoned
- 1990-09-06 EP EP90913267A patent/EP0445244B1/de not_active Expired - Lifetime
- 1990-09-06 AT AT90913267T patent/ATE128142T1/de not_active IP Right Cessation
- 1990-09-06 ES ES90913267T patent/ES2078351T3/es not_active Expired - Lifetime
- 1990-09-06 WO PCT/DE1990/000690 patent/WO1991004264A1/de active IP Right Grant
- 1990-09-06 DK DK90913267.2T patent/DK0445244T3/da active
- 1990-09-06 DE DE59009691T patent/DE59009691D1/de not_active Expired - Fee Related
- 1990-09-06 JP JP2512343A patent/JP2933713B2/ja not_active Expired - Lifetime
- 1990-09-06 US US07/721,608 patent/US5151533A/en not_active Expired - Fee Related
- 1990-09-18 DD DD90344084A patent/DD298107A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| WO1991004264A1 (de) | 1991-04-04 |
| EP0445244B1 (de) | 1995-09-20 |
| US5151533A (en) | 1992-09-29 |
| JP2933713B2 (ja) | 1999-08-16 |
| DK0445244T3 (da) | 1996-01-22 |
| EP0445244A1 (de) | 1991-09-11 |
| CA2042029A1 (en) | 1991-03-21 |
| ES2078351T3 (es) | 1995-12-16 |
| DE3931820A1 (de) | 1991-03-28 |
| JPH04505331A (ja) | 1992-09-17 |
| ATE128142T1 (de) | 1995-10-15 |
| DE59009691D1 (de) | 1995-10-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |