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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl chloroformate → [2-(3-Chloro-phenyl)-1-methyl-ethyl]-carbamic acid methyl ester

HRID 2277584
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HRID 2277584 반응식
Cl[C:2]([O:4][CH3:5])=[O:3].[Cl:6][C:7]1[CH:8]=[C:9]([CH2:13][CH:14]([NH2:16])[CH3:15])[CH:10]=[CH:11][CH:12]=1.C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[CH3:5][O:4][C:2](=[O:3])[NH:16][CH:14]([CH3:15])[CH2:13][C:9]1[CH:10]=[CH:11][CH:12]=[C:7]([Cl:6])[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6586Methyl chloroformateHCID 11430Potassium CarbonateHCID 20027470m-Chloroamphetamine

생성물 1

HCID 86685920[2-(3-Chloro-phenyl)-1-methyl-ethyl]-carbamic acid methyl ester수율 90%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

At 0° C., methyl chloroformate (0.67 g, 7.1 mmol) was added dropwise to a mixture of 2-(3-chloro-phenyl)-1-methyl-ethylamine (1.0 g, 5.9 mmol) and potassium carbonate (1.63 g, 11.8 mmol) in THF (20 mL). After the addition, the mixture was stirred at room temperature overnight. After filtration and evaporation of the volatiles, the crude product was purified by flash column chromatography (silica gel, 12 g, 50% hexane in dichloromethane) to give the title compound as a white solid (1.2 g, 90%). MS: 228.1 (M+H+).

후처리

  1. additionAfter the addition
  2. filtrationAfter filtration and evaporation of the volatiles
  3. customthe crude product was purified by flash column chromatography (silica gel, 12 g, 50% hexane in dichloromethane)

출처 및 근거

ORD 기록
ord-09a98024edda4cf28ca9444f163734bd
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133158B2

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