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Pregna-1,4,20-trien-3-one → Pregna-1,4,20-trien-3-ol

HRID 864363
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HRID 864363 반응식
[CH2:1]=[CH:2][C@@H:3]1[C@:20]2([CH3:21])[C@H:6]([C@H:7]3[C@H:17]([CH2:18][CH2:19]2)[C@:15]2([CH3:16])[C:10](=[CH:11][C:12](=[O:22])[CH:13]=[CH:14]2)[CH2:9][CH2:8]3)[CH2:5][CH2:4]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>CCOCC>[CH2:1]=[CH:2][C@@H:3]1[C@:20]2([CH3:21])[C@H:6]([C@H:7]3[C@H:17]([CH2:18][CH2:19]2)[C@:15]2([CH3:16])[C:10](=[CH:11][CH:12]([OH:22])[CH:13]=[CH:14]2)[CH2:9][CH2:8]3)[CH2:5][CH2:4]1
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참가 물질

4

반응물 2

HCID 13034987Pregna-1,4,20-trien-3-oneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 54245759Pregna-1,4,20-trien-3-ol수율 10%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Pregna-1,4,20-trien-3-one (3, 0.26 g, 088 mmol) in 25 mL of anh. ether was reduced under argon atmosphere with lithium aluminum hydride (250.5 mg, 6.601 mmol) for 2 h and then quenched with 2.50 g of Glauber's salt. The resulting suspension was stirred 70 min., filtered, and washed twice with 50 mL portions of ether. After concentrating the combined filtrates under reduced pressure the residue was purified using preparative TLC (35% ethyl acetate/hexanes on alumina to give white needles (26.1 mg, 87.4 μmol, 10%) m.p. 98°-128° C. (NA-1993B-81)

후처리

  1. customquenched with 2.50 g of Glauber's salt
  2. filtrationfiltered
  3. washwashed twice with 50 mL portions of ether
  4. concentrationAfter concentrating the combined filtrates under reduced pressure the residue
  5. customwas purified

출처 및 근거

ORD 기록
ord-48f0907bfbfc49f4965aa699c9abcab1
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05563131

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