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Phenethylamine → 3,4-dimethoxy-N-(2-phenylethyl)benzamide

HRID 1031899
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HRID 1031899 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:6]([OH:8])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.[C:26]1([CH2:32][CH2:33][NH2:34])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:6]([NH:34][CH2:33][CH2:32][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:8]
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참가 물질

5

반응물 3

HCID 1001PhenethylamineHCID 7121Veratric AcidHCID 682631,1'-Carbonyldiimidazole

생성물 1

HCID 8193303,4-dimethoxy-N-(2-phenylethyl)benzamide수율 65.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 3,4-dimethoxybenzoic acid (9.1 g, 0.05 mol) and carbonyldiimidazole (8.1 g, 0.05 mol) in 100 ml of THF was stirred for 3 h protected from moisture. The resulting solution was treated with 2-phenylethylamine (6.1 g, 0.05 mol) dissolved in 10 ml of THF. After 2 h of stirring, the solvent was evaporated and the solid residue was washed with dilute NaOH, dilute HCl, and water. The crude Al was recrystallized from 75 ml of EtOH to afford 9.35 g (57%) of N-(3,4-dimethoxybenzoyl)-2-phenylethylamine, mp 123-124°.

후처리

  1. customthe solvent was evaporated
  2. washthe solid residue was washed with dilute NaOH, dilute HCl, and water
  3. customThe crude Al was recrystallized from 75 ml of EtOH

출처 및 근거

ORD 기록
ord-0613482e43c74beeac06e7060a93b684
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04956371

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