Sodium Bicarbonate → (1R,2S)-1-cyano-2-hexyl-1-(4-hydroxyphenyl)cyclopropane

HRID 973514ノート

反応式

HRID 973514 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[C:5]([C@:7]1([C:16]2[CH:21]=[CH:20][C:19]([O:22]C)=[CH:18][CH:17]=2)[CH2:9][C@@H:8]1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])#[N:6].C(=O)([O-])O.[Na+]>CSC.ClCCl>[C:5]([C@:7]1([C:16]2[CH:17]=[CH:18][C:19]([OH:22])=[CH:20][CH:21]=2)[CH2:9][C@@H:8]1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])#[N:6]

参加物

6

実験手順

To a solution of 1.38 g (10.4 mmol) of aluminum chloride in 10 ml of dimethyl sulfide (Me2S) was added, with cooling with ice, a solution of 267 mg (1 mmol) of (1R,2S)-1-cyano-2-hexyl-1-(4-methoxyphenyl)cyclopropane in 10 ml of dichloromethane. This mixture was stirred with heating for 30 minutes. Saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, and the mixture was then subjected to extraction with 250 ml of ethyl acetate. The resulting ethyl acetate solution was washed with saturated sodium chloride aqueous solution, dried with anhydrous magnesium sulfate, and then concentrated. The residue was separated and purified by column chromatography (Kieselgel 60, hexane/ethyl acetate=5/1), thereby obtaining 197 mg (yield 81%) of (1R,2S)-1-cyano-2-hexyl-1-(4-hydroxyphenyl)cyclopropane.

後処理

  1. temperaturewith cooling with ice
  2. temperaturewith heating for 30 minutes
  3. extractionthe mixture was then subjected to extraction with 250 ml of ethyl acetate
  4. washThe resulting ethyl acetate solution was washed with saturated sodium chloride aqueous solution
  5. dry with materialdried with anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customThe residue was separated
  8. custompurified by column chromatography (Kieselgel 60, hexane/ethyl acetate=5/1)

出典と根拠

ORDレコード
ord-f822ac471ffa4d819c1217a8a474be12
出典データセット
uspto-grants-1991_11
特許番号
US05064564

反応ノート

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