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Nitromethane → tert-Butyl 3-hydroxy-3-(nitromethyl)azetidine-1-carboxylate

HRID 1803054
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HRID 1803054 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:11][C:10](=[O:12])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[N+:13]([CH3:16])([O-:15])=[O:14].C(N(CC)CC)C>C(O)C>[C:1]([O:5][C:6]([N:8]1[CH2:9][C:10]([OH:12])([CH2:16][N+:13]([O-:15])=[O:14])[CH2:11]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6375NitromethaneHCID 8471TriethylamineHCID 15194043-Oxo-azetidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 57415904tert-Butyl 3-hydroxy-3-(nitromethyl)azetidine-1-carboxylate수율 97%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3-Oxoazetidine-1-carboxylic acid tert-butyl ester (500 mg, 2.9 mmol) was dissolved in ethanol (1.5 mL) and to this was added nitromethane (0.6 mL) and triethylamine (cat.). The reaction was stirred for eighteen hours and the solvent was then removed under reduced pressure to yield the title compound as a white solid (650 mg, 97%). δH (d6-DMSO) 6.42 (1H, s), 4.86 (2H, s), 4.04 (2H, d, J 9.2 Hz), 3.75 (2H, d, J 9.2 Hz), 1.39 (9H, s). LCMS (ES+) RT (pH 10) 1.73 min (M−H)− 231.

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후처리

  1. customthe solvent was then removed under reduced pressure

출처 및 근거

ORD 기록
ord-2c39a6569bf747fd88d1edcfb9a6584b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08350037B2

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