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Piperidine → Methyl 3-(piperidin-1-ylmethyl)benzoate

HRID 35037
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HRID 35037 반응식
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Br[CH2:8][C:9]1[CH:10]=[C:11]([CH:16]=[CH:17][CH:18]=1)[C:12]([O:14][CH3:15])=[O:13]>C1(C)C=CC=CC=1>[N:1]1([CH2:8][C:9]2[CH:10]=[C:11]([CH:16]=[CH:17][CH:18]=2)[C:12]([O:14][CH3:15])=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8082PiperidineHCID 517981Methyl 3-(bromomethyl)benzoate

생성물 1

HCID 7162043Methyl 3-(piperidin-1-ylmethyl)benzoate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of piperidine (25 ml) and 3-(bromomethyl)benzoic acid, methyl ester (20 g) in toluene (600 ml) was stirred at room temperature for 4 h. The white preciptiate was removed by filtration and the filtrate was distilled to give the title compound as a colourless oil (17.56 g) b.p. 110° (10-1 mm). TLC silica; ether; Rf 0.7.

후처리

  1. customThe white preciptiate was removed by filtration
  2. distillationthe filtrate was distilled

출처 및 근거

ORD 기록
ord-d2db7d61cdb94d9a851edbff15c6518d
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04764612

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