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Diketene → 1-(1,3-Dioxobutyl)pyrrolidine

HRID 1055242
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HRID 1055242 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:6]=[C:7]1[O:11][C:9](=[O:10])[CH2:8]1>O1CCCC1>[N:1]1([C:9](=[O:10])[CH2:8][C:7](=[O:11])[CH3:6])[CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 12661DiketeneHCID 31268Pyrrolidine

생성물 1

HCID 1007221-(1,3-Dioxobutyl)pyrrolidine수율 81%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

A solution of 21 ml (0.25 mol) of pyrrolidine in 50 ml tetrahydrofuran was added dropwise to a solution of 20 g of diketene (0.24 mol) in 200 ml tetrahydrofuran at −5 to 0° C. After 1 h stirring at 0° C. no more starting material was detected by thin layer chromatography. The reaction mixture was evaporated and the residue was purified by column chromatography. This gave 29.9 g (0.19 mol, 81% yield) of an oil.

후처리

  1. customThe reaction mixture was evaporated
  2. customthe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-ec1e43e93ef64b4d883e00360b6ccd1c
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394324B2

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