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4-Fluorobenzylamine → HCID 67482556, 화합물

HRID 2402303
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인쇄 미리보기

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HRID 2402303 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=[O:12])[NH:5][C:6]2=[O:11].[F:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18]N)=[CH:16][CH:15]=1>C(O)(=O)C>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=[O:12])[N:5]([CH2:18][C:17]1[CH:20]=[CH:21][C:14]([F:13])=[CH:15][CH:16]=1)[C:6]2=[O:11]
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참가 물질

4

반응물 2

HCID 673264-FluorobenzylamineHCID 2312384-chloroisoindole-1,3-dione

생성물 1

HCID 67482556HCID 67482556, 화합물수율 89%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
150 °C

실험 절차

A mixture of 4-chloro-isoindole-1,3-dione (2.75 g, 15 mmol) and 4-fluorobenzylamine (1.88 g, 15 mmol) in glacial acetic acid (10 mL) was heated at 150° C. in microwave for 30 mins. After cooled to room temperature, the reaction mixture was poured into ice water and the white precipitates were collected. Recrystallization with EtOH provided the title compound (3.86 g, 89%).

후처리

  1. temperatureAfter cooled to room temperature
  2. customthe white precipitates
  3. customwere collected
  4. customRecrystallization with EtOH

출처 및 근거

ORD 기록
ord-f8c12a5b93474e49a8919040bfbe3b97
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796313B2

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