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(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester → (R)-(S)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester

HRID 1261807
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반응식

HRID 1261807 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@@H:10]([CH:13]2[CH2:15][O:14]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>O>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@@H:10]([C@H:13]2[CH2:15][O:14]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86664072(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester

생성물 1

HCID 86664073(R)-(S)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester

시약·촉매·용매 1

HCID 962Water용매

실험 절차

(R)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester (30 g, 140.6 mmol, 1.0 eq.) was combined with (S,S)-Salen Co(II) (418 mg, 0.7 mmol). Water (⅓ mL) was added and the resulting mixture was stirred vigorously for 6 hours. Hexanes (200 mL) was added. The resulting solids were crushed and stirred in hexanes to yield a yellow precipitate. The precipitate was purified by column chromatography (200-300 mesh, hexanes:EtOAc=1:3, 3 L) to yield (R)-(S)-3-Oxiranylpyrrolidine-1-carboxylic acid t-butyl ester.

후처리

  1. customThe resulting solids were crushed
  2. custom
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
to yield a yellow precipitate
  • customThe precipitate was purified by column chromatography (200-300 mesh, hexanes:EtOAc=1:3, 3 L)
  • 출처 및 근거

    ORD 기록
    ord-afe829a555bd472e93a6d4c0fda7a4ce
    출처 데이터셋
    uspto-grants-2013_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08471040B2

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