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Dimethylamine → Methyl 2-benzyl-3-dimethylaminopropionate

HRID 621610
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인쇄 미리보기

반응식

HRID 621610 반응식
[CH2:1]([C:8](=[CH2:13])[C:9]([O:11][CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:14][NH:15][CH3:16]>CO>[CH2:1]([CH:8]([CH2:13][N:15]([CH3:16])[CH3:14])[C:9]([O:11][CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 575761Methyl 2-benzylprop-2-enoate

생성물 1

HCID 13653933Methyl 2-benzyl-3-dimethylaminopropionate

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of 30.0 g of methyl α-benzylacrylate, prepared by the method of R. B. Miller and B. F. Smith, Synth. Commun. 3, 359 (1973) in methanol (50 ml) is added to a solution of dimethylamine (71.0 g) in methanol (210 ml), and the mixture is stirred at room temperature for b 48 hours. The solvent is removed under reduced pressure to give methyl 2-benzyl-3-dimethylaminopropionate as a yellow oil, used without purification in the next synthetic step; NMR: δ7.14 (s, 5H), 3.52 (s, 3H), 2.82 (m, 3H), 2.17 (s, 6H), 2.63-2.17 (m, remaining H).

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후처리

  1. customThe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-ad41d0bcc30340d69dd3450b36dca77b
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824868

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