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Water → (3S,4S)-4-(1-(R)-carboxyethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone

HRID 21720
ノート
印刷プレビュー

反応式

HRID 21720 の反応式
[OH:1][CH2:2][C@@H:3]([C@@H:5]1[NH:8][C:7](=[O:9])[C@@H:6]1[C@H:10]([O:12][C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14])[CH3:11])[CH3:4].CC(C)=[O:25].OS(O)(=O)=O.O=[Cr](=O)=O.S(=O)(=O)(O)O.O>CC(C)=O.[O-2].[O-2].[O-2].[Cr+6]>[C:2]([C@@H:3]([C@H:5]1[NH:8][C:7](=[O:9])[C@@H:6]1[C@H:10]([O:12][C:13]([O:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)=[O:14])[CH3:11])[CH3:4])([OH:25])=[O:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 1118Sulfuric AcidHCID 13960427(3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinoneHCID 131709961Jones' reagent

生成物 1

HCID 13960430(3S,4S)-4-(1-(R)-carboxyethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone

試薬・触媒・溶媒 2

HCID 10219390
chromium (VI) trioxide
触媒
HCID 180Acetone溶媒

実験手順

A solution of (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone (6.1 g) in acetone (60 ml) was treated with the Jones reagent, prepared from chromium trioxide (2.78 g), 98% sulfuric acid (4.4 g) and water (8.1 ml), at 10°-20° C. for 1 hour. The reaction mixture was quenched with isopropanol (0.5 ml) at 10°-20° C. for 15 minutes, diluted with ethyl acetate (122 ml) and washed with water (135 ml). The aqueous layer was separated from the organic layer and extracted with ethyl acetate (61 ml). The ethyl acetate extracts and the organic layer were combined together and extracted with 5% aqueous sodium bicarbonate solution (30 ml). The extract was washed with dichloromethane (60 ml) and acidified with 10% hydrochloric acid solution (20 ml) with ice-cooling. The acidic solution was extracted twice with dichloromethane (60 ml). The extracts were washed with brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated in vacuo to give (3S,4S)-4-(1-(R)-carboxyethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone.

後処理

  1. customThe reaction mixture was quenched with isopropanol (0.5 ml) at 10°-20° C. for 15 minutes
  2. additiondiluted with ethyl acetate (122 ml)
  3. washwashed with water (135 ml)
  4. customThe aqueous layer was separated from the organic layer
  5. extractionextracted with ethyl acetate (61 ml)
  6. extractionextracted with 5% aqueous sodium bicarbonate solution (30 ml)
  7. washThe extract was washed with dichloromethane (60 ml)
  8. temperaturecooling
  9. extractionThe acidic solution was extracted twice with dichloromethane (60 ml)
  10. washThe extracts were washed with brine
  11. dry with materialdried over anhydrous sodium sulfate
  12. filtrationAfter filtration
  13. concentrationthe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-b76297b7782a4dedb693a126d3a0daab
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05424422

反応ノート

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