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m-Chloroperbenzoic acid → 3-hydroxy-4-[(2S)-oxiranylmethoxy]-9H-carbazole

HRID 1634716
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HRID 1634716 반응식
[O:1]1[CH2:3][C@H:2]1[CH2:4][O:5][C:6]1[C:18]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]=2[CH:9]=[CH:8][CH:7]=1.ClC1C=CC=C(C(OO)=[O:27])C=1>C(Cl)Cl>[OH:27][C:7]1[CH:8]=[CH:9][C:10]2[NH:11][C:12]3[C:17]([C:18]=2[C:6]=1[O:5][CH2:4][C@@H:2]1[CH2:3][O:1]1)=[CH:16][CH:15]=[CH:14][CH:13]=3
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 10879208(S)-(+)-4-(2,3-Epoxypropoxy)carbazole

생성물 1

HCID 590329483-hydroxy-4-[(2S)-oxiranylmethoxy]-9H-carbazole수율 20.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 4-[(2S)-oxiranylmethoxy]-9H-carbazole (0.183 g, 0.76 mmol) in 20 mL dry methylene chloride was treated with 0.258 g of 56-86% m-chloroperbenzoic acid. The reaction was stirred at ambient temperature for 45 minutes. The reaction mixture was partitioned with saturated sodium bicarbonate (sat'd NaHCO3) The organic phase was dried (Na2SO4) and concentrated to a dark red oil. Purification by flash chromatography eluting with methylene chloride (CH2Cl2), afforded 0.040 g of the title compound.

후처리

  1. customThe reaction mixture was partitioned with saturated sodium bicarbonate (sat'd NaHCO3) The organic phase
  2. dry with materialwas dried (Na2SO4)
  3. concentrationconcentrated to a dark red oil
  4. customPurification by flash chromatography
  5. washeluting with methylene chloride (CH2Cl2)

출처 및 근거

ORD 기록
ord-46857b66505c4a4b8c4d710c4e23fa0a
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06506901B2

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