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N-Methylaniline → Ethyl 5-[methyl(phenyl)amino]pentanoate

HRID 2225895
노트
인쇄 미리보기

반응식

HRID 2225895 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15].C(=O)(O)[O-].[Na+]>>[CH3:1][N:2]([CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7515N-MethylanilineHCID 84580Ethyl 5-bromovalerateHCID 516892Sodium Bicarbonate

생성물 1

HCID 19438629Ethyl 5-[methyl(phenyl)amino]pentanoate수율 84.1%

반응 조건

온도
110 °C

실험 절차

A mixture of N-methylaniline (16 g) and ethyl 5-bromovalerate (30.2 g) was stirred at 110° C. for 22 hours. Then the mixture was made alkaline with an aqueous sodium bicarbonate. The resulting mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate and concentrated. The residue was distilled under reduced pressure to obtain ethyl 5-(N-methylanilino)valerate (28.6 g).

후처리

  1. extractionThe resulting mixture was extracted with ethyl acetate
  2. dry with materialdried over anhydrous magnesium sulfate
  3. concentrationconcentrated
  4. distillationThe residue was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-b4bbe2adf4c64a9e8b088fcf64822498
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05344928

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