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

Piperazine → (3-Oxo-6-cyclohexyl-1-cyclohexen-1-yl)-piperazine

HRID 980825
노트
인쇄 미리보기

반응식

HRID 980825 반응식
O=[C:2]1[CH:7]([CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)[CH2:6][CH2:5][C:4](=[O:14])[CH2:3]1.[NH:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1>C1(C)C=CC=CC=1>[O:14]=[C:4]1[CH2:5][CH2:6][CH:7]([CH:8]2[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]2)[C:2]([N:15]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)=[CH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4837PiperazineHCID 202209951,3-Dioxo-6-cyclohexyl-cyclohexane

생성물 1

HCID 13520892(3-Oxo-6-cyclohexyl-1-cyclohexen-1-yl)-piperazine수율 76%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 9.8 g (0.05 mol) of 1,3-dioxo-6-cyclohexyl-cyclohexane, 12.9 g (0.15 mol) of anhydrous piperazine and 150 ml of toluene is reacted and worked up as described in Example 1. For purification, column chromatography is included (corresponding to Example 2). (3-Oxo-6-cyclohexyl-1-cyclohexen-1-yl)-piperazine is obtained as an oil in an amount of 9.9 g (=76% yield) with an RF value of 0.36 (conditions corresponding to Example 1). The dihydrochloride has a melting point of 258°-261° C. (decomposition).

후처리

  1. customis reacted
  2. customFor purification, column chromatography

출처 및 근거

ORD 기록
ord-e0ab47994d4d4983a859060b065cf16e
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04639453

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트