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Benzoyl chloride → 15alpha-Benzoyloxyestra-4,9-diene-3,17-dione

HRID 329382
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HRID 329382 반응식
[OH:1][C@@H:2]1[C@H:7]2[C@H:8]3[C:17]([CH2:18][CH2:19][C@:5]2([CH3:6])[C:4](=[O:21])[CH2:3]1)=[C:16]1[C:11](=[CH:12][C:13](=[O:20])[CH2:14][CH2:15]1)[CH2:10][CH2:9]3.[C:22](Cl)(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>N1C=CC=CC=1>[C:22]([O:1][C@@H:2]1[C@H:7]2[C@H:8]3[C:17]([CH2:18][CH2:19][C@:5]2([CH3:6])[C:4](=[O:21])[CH2:3]1)=[C:16]1[C:11](=[CH:12][C:13](=[O:20])[CH2:14][CH2:15]1)[CH2:10][CH2:9]3)(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
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참가 물질

4

반응물 2

HCID 7412Benzoyl chlorideHCID 1342360815alpha-Hydroxy-4,9-estradiene-3,17-dione

생성물 1

HCID 5661194015alpha-Benzoyloxyestra-4,9-diene-3,17-dione

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A solution of 20 g of 15α-hydroxyestra-4,9-diene-3,17-dione in 120 ml of pyridine is combined dropwise with 13.6 ml of benzoyl chloride and the mixture is stirred for one hour at room temperature. Subsequently the mixture is poured into ice water, extracted with dichloromethane, washed with sodium bicarbonate solution and water and concentrated under vacuum. The cooled crude product is chromatographed on silica gel, yielding 26.2 g of 15α-benzoyloxyestra-4,9-diene-3,17-dione.

후처리

  1. extractionextracted with dichloromethane
  2. washwashed with sodium bicarbonate solution and water
  3. concentrationconcentrated under vacuum
  4. temperatureThe cooled crude product
  5. customis chromatographed on silica gel

출처 및 근거

ORD 기록
ord-6f4ee7e382d24588bccd527460a495cb
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04891365

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