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Water → Cyclopropanecarboxylic acid(5-bromo-2-iodo-benzyl)-ethyl-amide

HRID 1625673
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HRID 1625673 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([I:12])=[C:6]([CH:11]=1)[CH2:7][NH:8][CH2:9][CH3:10].C(N(CC)C(C)C)(C)C.[CH:22]1([C:25](Cl)=[O:26])[CH2:24][CH2:23]1.O>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([I:12])=[C:6]([CH:11]=1)[CH2:7][N:8]([CH2:9][CH3:10])[C:25]([CH:22]1[CH2:24][CH2:23]1)=[O:26]
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참가 물질

6

반응물 4

HCID 962WaterHCID 77637Cyclopropanecarbonyl chlorideHCID 81531DiisopropylethylamineHCID 58148919(5-Bromo-2-iodo-benzyl)-ethyl-amine

생성물 1

HCID 58149034Cyclopropanecarboxylic acid(5-bromo-2-iodo-benzyl)-ethyl-amide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

(5-Bromo-2-iodo-benzyl)-ethyl-amine (5.0 g, 14.7 mmol) was dissolved in dichloromethane (75 mL) along with N,N-diisopropylethylamine (5.12 mL, 29.4 mmol). The solution was cooled to 0° C. and cyclopropanecarbonyl chloride (1.41 mL, 15.4 mmol) was added. The reaction was monitored by analytical LCMS and after 15 minutes water was added and the layers were separated. The organic layer was dried with magnesium sulfate then filtered and concentrated to afford the title compound, which was used without further purification.

후처리

  1. customthe layers were separated
  2. dry with materialThe organic layer was dried with magnesium sulfate
  3. filtrationthen filtered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-25da86860178472eb61874c672942ef6
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785393B2

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