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Water → N-(4-bromo-2-isopropylphenyl)acetamide

HRID 1170954
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HRID 1170954 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([CH:9]([CH3:11])[CH3:10])[CH:3]=1.O.[C:13](OC(=O)C)(=[O:15])[CH3:14]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:13](=[O:15])[CH3:14])=[C:4]([CH:9]([CH3:11])[CH3:10])[CH:3]=1
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참가 물질

4

반응물 3

HCID 962WaterHCID 7918Acetic AnhydrideHCID 222719374-Bromo-2-(propan-2-yl)aniline

생성물 1

HCID 20351194N-(4-bromo-2-isopropylphenyl)acetamide수율 83%

실험 절차

A solution of 4-bromo-2-iso-propyl-phenylamine (780 mg, 3.64 mmol) in acetic anhydride (4 mL) was stirred at room temperature over night. The reaction was poured into water and the resulting white precipitate was filtered off and dried under vacuum to give N-(4-bromo-2-iso-propyl-phenyl)-acetamide as a light pink solid (0.770 g, 83%); 1H NMR (300 MHz, DMSO-d6): δ 9.39 (s, 1H), 7.43 (d, 1H, J=2.4 Hz), 3.16 (m, 1H), 2.04 (s, 3H), 1.13 (d, 6H, J=7 Hz); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=dichloromethane; Rf=0.21

후처리

  1. filtrationthe resulting white precipitate was filtered off
  2. customdried under vacuum

출처 및 근거

ORD 기록
ord-8d4a42d9ab514bc1a39e308b656ad827
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829552B2

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