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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Bromoaniline → N-(4-Bromophenyl)-3-oxobutanamide

HRID 2112809
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HRID 2112809 반응식
[CH2:1]=[C:2]1[O:6][C:4](=[O:5])[CH2:3]1.[Br:7][C:8]1[CH:14]=[CH:13][C:11]([NH2:12])=[CH:10][CH:9]=1>C1(C)C=CC=CC=1>[Br:7][C:8]1[CH:14]=[CH:13][C:11]([NH:12][C:4](=[O:5])[CH2:3][C:2](=[O:6])[CH3:1])=[CH:10][CH:9]=1
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참가 물질

4

반응물 2

HCID 78074-BromoanilineHCID 12661Diketene

생성물 1

HCID 598820N-(4-Bromophenyl)-3-oxobutanamide

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

A solution of 25.72 mL (336 mmol) of diketene in 100 mL of toluene is added dropwise at 90° C. to a solution of 51.0 g (288 mmol) of 4-bromoaniline in 200 mL of toluene and the reaction mixture is kept for 5 hours at this temperature. The reaction solution is cooled in the ice bath, and the precipitate formed is filtered and then washed with toluene until the product is virtually colorless. Subsequently it is dried at 50° C. in the circulating air dryer until the weight is constant. Yield: 50.0 g (68% of theoretical); C10H10BrNO2 (M=256.096); calc.: molpeak (M+H)+: 256/258 (Br); found: molpeak (M+H)+: 256/258 (Br); HPLC-MS: 4.7 min (method B).

후처리

  1. customthe precipitate formed
  2. filtrationis filtered
  3. washwashed with toluene until the product
  4. customSubsequently it is dried at 50° C. in the circulating air dryer until the weight
  5. custom4.7 min (method B)

출처 및 근거

ORD 기록
ord-c5ddacf3307643809bb7889ce93f0956
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07524862B2

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