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4-Fluorobenzylamine → 2-Pyrrolidinone, 1-((4-fluorophenyl)methyl)-

HRID 426951
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HRID 426951 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH2:7])=[CH:4][CH:3]=1.[O:10]1[CH:14]=[CH:13][CH2:12][C:11]1=O>C1(C=CC(O)=CC=1)O>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][N:7]2[CH2:14][CH2:13][CH2:12][C:11]2=[O:10])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 673264-FluorobenzylamineHCID 1407652(3H)-Furanone

생성물 1

HCID 30454462-Pyrrolidinone, 1-((4-fluorophenyl)methyl)-수율 74.8%

시약·촉매·용매 1

HCID 785Hydroquinone촉매

실험 절차

47 g (0.376 mol) of p-fluorobenzylamine, 30.4 g (0.353 mol) of furan-2-one and 0.4 g of hydroquinone are introduced into a 125 ml autoclave. After driving the air out of the apparatus by passing a stream of nitrogen through it, the mixture is heated to 250° for 6 hours. It is then cooled and distilled under reduced pressure. 51 g (yield=74.8%) of 1-p-fluorobenzyl-pyrrolidin-2-one are collected as a colourless liquid distilling at 103°-105° under a pressure of 0.01 mm of mercury and solidifying slowly. Melting point=37°-38°.

후처리

  1. temperaturethe mixture is heated to 250° for 6 hours
  2. temperatureIt is then cooled
  3. distillationdistilled under reduced pressure

출처 및 근거

ORD 기록
ord-a46083d02c5a416d934728269f0c973d
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04172143

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