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1,1-Dimethylethyl N-[2-[(4-chlorobenzoyl)amino]ethyl]carbamate → N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride

HRID 2255102
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HRID 2255102 반응식
[Cl:1][C:2]1[CH:20]=[CH:19][C:5]([C:6]([NH:8][CH2:9][CH2:10][NH:11]C(=O)OC(C)(C)C)=[O:7])=[CH:4][CH:3]=1>C(O)=O>[ClH:1].[NH2:11][CH2:10][CH2:9][NH:8][C:6](=[O:7])[C:5]1[CH:19]=[CH:20][C:2]([Cl:1])=[CH:3][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 135768931,1-Dimethylethyl N-[2-[(4-chlorobenzoyl)amino]ethyl]carbamate

생성물 1

HCID 5702251N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride수율 190.6%

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

A solution of 2.8 g of t-butyl [2-(4-chlorobenzamido)ethyl]carbamate in 50 ml of formic acid is left to stand at room temperature for 1.5 hours. The mixture is then concentrated to dryness, and the residue is dissolved in 50 ml of hydrochloric acid(l:l; volume/volume). The solution is concentrated, the residue is evaporated twice with ethanol/benzene and then recrystallized from ethanol. There are obtained 2.1 g of N-(2-aminoethyl)-4-chlorobenzamide hydrochloride which is identical with the product obtained in Example 1.

후처리

  1. concentration
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The mixture is then concentrated to dryness
  • dissolutionthe residue is dissolved in 50 ml of hydrochloric acid(l:l; volume/volume)
  • concentrationThe solution is concentrated
  • customthe residue is evaporated twice with ethanol/benzene
  • customrecrystallized from ethanol
  • 출처 및 근거

    ORD 기록
    ord-efdf32f9ee6c4804ab65832f207c47f4
    출처 데이터셋
    uspto-grants-1993_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05238962

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