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

Dicyclohexylamine → N,N-Diethyl-5-[6-[(6-bromohexyl)oxy]-1-hexynyl]-2-furancarboxamide

HRID 1086901
노트
인쇄 미리보기

반응식

HRID 1086901 반응식
[CH2:1]([N:3]([CH2:12][CH3:13])[C:4]([C:6]1[O:7][C:8](Br)=[CH:9][CH:10]=1)=[O:5])[CH3:2].[Br:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]#[CH:27].C1(NC2CCCCC2)CCCCC1>>[CH2:1]([N:3]([CH2:12][CH3:13])[C:4]([C:6]1[O:7][C:8]([C:27]#[C:26][CH2:25][CH2:24][CH2:23][CH2:22][O:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][Br:14])=[CH:9][CH:10]=1)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7582DicyclohexylamineHCID 9323705-bromo-N,N-diethyl-2-furamideHCID 218671586-[(6-Bromohexyl)oxy]-1-hexyne

생성물 1

HCID 19818694N,N-Diethyl-5-[6-[(6-bromohexyl)oxy]-1-hexynyl]-2-furancarboxamide수율 73.2%

실험 절차

N,N-diethyl-5-bromo-2-furancarboxamide (1.5 g) was treated with 6-[(6-bromohexyl)oxy]-1-hexyne (1.59 g) and N,N-dicyclohexylamine (2.10 g) according to the method of Intermediate 9 except that the reaction mixture was refluxed under nitrogen for 3 h and FCC eluting with hexane followed by hexane:ether (4:1→1:1) gave the title compound as an orange oil (1.90 g), t.l.c. (hexane:ether 1:1) Rf 0.15.

후처리

  1. temperaturewas refluxed under nitrogen for 3 h
  2. washFCC eluting with hexane

출처 및 근거

ORD 기록
ord-c965195ad5c34e3b87f98eb0c8ac3025
출처 데이터셋
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05032609

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트