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Bromine → N-(4-Bromo-3-chloro-2-methylphenyl)acetamide

HRID 1157663
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인쇄 미리보기

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HRID 1157663 반응식
[Cl:1][C:2]1[C:3]([CH3:12])=[C:4]([NH:8][C:9](=[O:11])[CH3:10])[CH:5]=[CH:6][CH:7]=1.[Br:13]Br>C(O)(=O)C>[Br:13][C:7]1[CH:6]=[CH:5][C:4]([NH:8][C:9](=[O:11])[CH3:10])=[C:3]([CH3:12])[C:2]=1[Cl:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 81969N-(3-chloro-2-methylphenyl)acetamide

생성물 1

HCID 86376N-(4-Bromo-3-chloro-2-methylphenyl)acetamide수율 93.6%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
0 °C

실험 절차

Dissolve N-(3-chloro-2-methyl-phenyl)-acetamide (120.0 g, 0.653 mol) in acetic acid and cool to 0° C. Add bromine (313.3 g, 1.96 mol) dropwise over 30 min via an addition funnel. Stir for 17 h while allowing the reaction to warm to room temperature. Pour the reaction into 1 L of ice, and filter. Rinse the filter cake with 4 L of water. The title product is isolated in 93.6% yield (160.6 g) as a white solid. MS: MS (ESI−): 262 (M−1)−. MS (ESI+): 263 (M+1)+.

후처리

  1. customthe reaction
  2. temperatureto warm to room temperature
  3. additionPour
  4. filtrationfilter
  5. washRinse the filter cake with 4 L of water

출처 및 근거

ORD 기록
ord-d9d9c2b6c46f4c54b4b8b8dd8b802dde
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07807691B2

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