참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Heptane | HCID 8900 | — |
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | 9alpha-Hydroxyandrost-4-ene-3,17-dione | HCID 10425017 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 9-Dehydroandrostenedione | HCID 239595 | — |
반응 단계
9α-Hydroxyandrostenedione (5.00 g.) is dissolved in methylene chloride (50 ml.) and cooled to 0°-5°. A solution of chlorosulfonic acid (2.5 ml.) in methylene chloride (10 ml.) is added slowly over a period of 4 minutes. At the end of the addition TLC shows the reaction is completed. Water (60 ml.) is added to the reaction mixture keeping the temperature at 3°-15°. The mixture is stirred for 2 minutes and heptane (135 ml.) is added. The organic phase is separated and washed twice with water (30 ml. each time). The organic phase is concentrated with heat to about 30 ml. with crystals forming as the solution cools. The mixture is cooled to 0°-5°, filtered, washed with a minimum amount of heptane, and dried at 70° to give androsta-4,9(11)-diene-3,17-dione; 4.45 g. (89.0% weight yield, 94.7% chemical yield), m.p., 195.5°-202°; [α]D +220° (chloroform); UV (methanol) λmax =240 nm (ε=16,300).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE033364 |
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| 출처 데이터셋 | uspto-grants-1990_10 |
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| ORD ID | ord-833163a22a864aeb9e9397e1b01d537d |
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| 출처 메모 | uspto-grants-1990_10 |
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