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Benzyl chloroformate → Phenylmethyl 2-[2-(acetyloxy)ethyl]-4-morpholinecarboxylate

HRID 1608218
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인쇄 미리보기

반응식

HRID 1608218 반응식
[C:1]([O:4][CH2:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][N:9](CC2C=CC=CC=2)[CH2:8]1)(=[O:3])[CH3:2].Cl[C:21]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22]>C(#N)C>[C:1]([O:4][CH2:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][N:9]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:8]1)(=[O:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 10387Benzyl chloroformateHCID 19848591HCID 19848591, 화합물

생성물 1

HCID 19848607Phenylmethyl 2-[2-(acetyloxy)ethyl]-4-morpholinecarboxylate수율 72.1%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 2-(2-acetoxyethyl)-4-benzylmorpholine (29.1 g) in acetonitrile (200 ml) is dropwise added benzyl chloroformate (24.4 g). The reaction mixture is refluxed for 30 minutes, cooled and evaporated under reduced pressure. The residue is chromatographed on silica gel. The eluate with hexane is discarded, and the subsequent eluates with hexane-chloroform (1:1) are pooled and evaporated to give the title compound (24.5 g) as an oil.

후처리

  1. temperatureThe reaction mixture is refluxed for 30 minutes
  2. temperaturecooled
  3. customevaporated under reduced pressure
  4. customThe residue is chromatographed on silica gel
  5. customevaporated

출처 및 근거

ORD 기록
ord-2961411c83ec4e38a426bdaa666b84c8
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04870074

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