(1S,2S)-1,2-diphenylethane-1,2-diamine → (R)-(Cyclopropyl)(2-methylphenyl)methanol

HRID 1349449

反応式

HRID 1349449 の反応式
C1([C@H](N)[C@H](C2C=CC=CC=2)N)C=CC=CC=1.CC(C)([O-])C.[K+].[CH3:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[C:30]([CH:32]1[CH2:34][CH2:33]1)=[O:31]>C(O)(C)C>[CH:32]1([C@H:30]([C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=2[CH3:23])[OH:31])[CH2:33][CH2:34]1

参加物

5

反応物 3

HCID 6931238(1S,2S)-1,2-diphenylethane-1,2-diamineHCID 22382440Cyclopropyl(2-methylphenyl)methanoneHCID 23665647Potassium tert-butoxide

生成物 1

HCID 60017546(R)-(Cyclopropyl)(2-methylphenyl)methanol収率 71.1%

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

実験手順

To a suspension of dichloro[(S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl]ruthenium(II) (851 mg), (1S,2S)-(−)-1,2-diphenyethylenediamine (191 mg) and potassium-tert-butoxide (270 mg) in isopropanol (90 ml) was added cyclopropyl 2-methylphenyl ketone (9.61 g) obtained in Step 2, and the mixture was hydrogenated at room temperature and at medium pressure (3.0 kgf/cm2) for 60 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9) to give the title compound (6.92 g).

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9)

出典と根拠

ORDレコード
ord-980cd5f8a7c548168c8e11f383650c71
出典データセット
uspto-grants-2007_05
特許番号
US07211685B2

関連ノート

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