Bicarbonate Ion → 7alpha-(5-Chloropentyl)-estr-4-ene-3,17-dione

HRID 361662ノート

反応式

HRID 361662 の反応式
O[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C@@H:7]1[CH2:24][C:23]2[C@H:18]([CH2:19][CH2:20][C:21](=[O:25])[CH:22]=2)[C@@H:17]2[C@@H:8]1[C@H:9]1[C@@:13]([CH2:15][CH2:16]2)([CH3:14])[C:12](=[O:26])[CH2:11][CH2:10]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(=O)(O)[O-].C(Cl)(Cl)(Cl)[Cl:51]>C(#N)C.ClCCl>[Cl:51][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C@@H:7]1[CH2:24][C:23]2[C@H:18]([CH2:19][CH2:20][C:21](=[O:25])[CH:22]=2)[C@@H:17]2[C@@H:8]1[C@H:9]1[C@@:13]([CH2:15][CH2:16]2)([CH3:14])[C:12](=[O:26])[CH2:11][CH2:10]1

参加物

7

反応物 4

HCID 769Bicarbonate IonHCID 5943Carbon TetrachlorideHCID 11776TriphenylphosphineHCID 158381567a-(5-Hydroxypentyl)-estr-4-ene-3,17-dione

生成物 1

HCID 571565697alpha-(5-Chloropentyl)-estr-4-ene-3,17-dione

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 6344Dichloromethane溶媒

実験手順

The same product is obtained from 8.05 g of 7α-(5-hydroxypentyl)-estr-4-ene-3,17-dione (Example 1b) by a 3.5-hour reaction with 8.66 g of triphenylphosphine in 85 ml of carbon tetrachloride and 30 ml of acetonitrile at room temperature. The reaction mixture is diluted with dichloromethane, shaken out with saturated bicarbonate solution and with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel with dichloromethane and ethyl acetate, whereby 4.08 g of 7α-(5-chloropentyl)-estr-4-ene-3,17-dione is obtained, [α]D22 =+68°(c=0.5% in chloroform)

後処理

  1. dry with materialdried with sodium sulfate
  2. concentrationconcentrated by evaporation in a vacuum
  3. customThe residue is chromatographed on silica gel with dichloromethane and ethyl acetate

出典と根拠

ORDレコード
ord-8997c68cba6e4c99863c1eff4e5a70ec
出典データセット
uspto-grants-1999_02
特許番号
US05866560

反応ノート

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