참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Methyl (17beta)-3-oxoandrost-4-ene-17-carboxylate | HCID 165014 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (17beta)-3-Oxoandrost-4-ene-17-carboxylic acid | HCID 99472 | 98% |
반응 단계
To 2.462 kg. of methyl 4-androsten-3-one-17β-carboxylate in 24.6 l of methanol was added 1.23 kg. of potassium hydroxide in 4.9 l. of water. The reaction mixture was refluxed under nitrogen for 6 hours, and then allowed to cool to room temperature overnight. The mixture was acidified with 3200 ml. of 6 N hydrochloric acid. Most of the product crystallized as fine crystals. Then, 14 l. of water was added in a stream over 30 minutes, which precipitated all of the product. The mixture was aged with stirring for 4 hours at 30° C. The mixture was filtered on a cap funnel and washed with water until the wash water showed neutral. The product was dried in an oven at 50° C. overnight. The product, having a m.p. of 245°-248° C., was obtained in 98% yield (2.313 g.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04220775 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-f656206c35324b4c97d16d00d8b85396 |
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| 출처 메모 | uspto-grants-1980_09 |
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