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Water → (1-hydroxymethyl-cyclopentyl)-carbamic Acid Benzyl Ester

HRID 855865
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반응식

HRID 855865 반응식
[NH2:1][C:2]1([CH2:7][OH:8])[CH2:6][CH2:5][CH2:4][CH2:3]1.C([O-])(O)=O.[Na+].O.[C:15](=O)([O:24]N1C(=O)CCC1=O)[O:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CC(C)=O>[CH2:17]([O:16][C:15](=[O:24])[NH:1][C:2]1([CH2:7][OH:8])[CH2:6][CH2:5][CH2:4][CH2:3]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 663071-AminocyclopentanemethanolHCID 83172Benzyl succinimido carbonateHCID 516892Sodium Bicarbonate

생성물 1

HCID 11557863(1-hydroxymethyl-cyclopentyl)-carbamic Acid Benzyl Ester

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a stirred solution of 1-amino-1-cyclopentanemethanol (1.15 g, 10 mmol) and NaHCO3 (0.84 g, 10 mmol) in acetone (14 mL)/water (14 ml) at room temperature was added benzyl succinimidyl carbonate (2.5 g, 10 mmol). The reaction mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and purified by flash chromatography with 3% methanol:dichloromethane to provide the titled compound. MS (DCI) m/z 250 (M+H)+.

후처리

  1. concentrationconcentrated under reduced pressure
  2. custompurified by flash chromatography with 3% methanol

출처 및 근거

ORD 기록
ord-24e100754a684d5ba753b1b0114b6006
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262207B2

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