홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Triethylamine → HCID 9862404, 화합물

HRID 1756020
노트
인쇄 미리보기

반응식

HRID 1756020 반응식
[CH:1]1([NH:7][C:8](=[O:17])[CH:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)Br)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:18]([NH:22][CH2:23][CH2:24][NH2:25])([CH3:21])([CH3:20])[CH3:19].C(N(CC)CC)C>C1(C)C=CC=CC=1>[CH:1]1([NH:7][C:8](=[O:17])[CH:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[NH:25][CH2:24][CH2:23][NH:22][C:18]([CH3:21])([CH3:20])[CH3:19])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10469811HCID 10469811, 화합물HCID 12504477N1-tert-butylethane-1,2-diamine

생성물 1

HCID 9862404HCID 9862404, 화합물수율 38.9%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of N-cyclohexyl-α-bromophenylacetamide (2.37 g), N-tert-butylethylenediamine (2.00 g), triethylamine (1.12 ml) and toluene (30 ml) was refluxed for 18 hours. The reaction mixture was concentrated and the residue was purified by means of alumina column chromatography (developing solvent, ethyl acetate) and then distilled under reduced pressure to obtain 1.03 g (38.9%) of title compound as a colorless oily product.

후처리

  1. temperaturewas refluxed for 18 hours
  2. concentrationThe reaction mixture was concentrated
  3. customthe residue was purified by means of alumina column chromatography (developing solvent, ethyl acetate)
  4. distillationdistilled under reduced pressure

출처 및 근거

ORD 기록
ord-46f911cf9d394a2892e20dc148aed74c
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05439919

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트