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

4,6,6-Trimethyl-1,3-cyclohexadiene-1-carboxaldehyde → 4,6,6-Trimethylcyclohex-1-ene-1-carbaldehyde

HRID 566851
노트
인쇄 미리보기

반응식

HRID 566851 반응식
[CH3:1][C:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[C:5]([CH:10]=[O:11])=[CH:4][CH:3]=1>[Pd].C(O)C>[CH3:1][CH:2]1[CH2:7][C:6]([CH3:8])([CH3:9])[C:5]([CH:10]=[O:11])=[CH:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 109206834,6,6-Trimethyl-1,3-cyclohexadiene-1-carboxaldehyde

생성물 1

HCID 212637424,6,6-Trimethylcyclohex-1-ene-1-carbaldehyde수율 87.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 4,6,6-trimethyl-1,3-cyclohexadiene-1-carbaldehyde (141 g, 0.94 mole), ethanol (1 l) and palladium on charcoal (10%, 0.5 g) was hydrogenated by shaking under a H2-atmosphere for 3.5 h. The H2-consumption was 23.5 l. After filtration and concentration of the thus-obtained solution, the residue was distilled at 50°/0.7 hPa, to obtain 125.3 g (87.6%) of the desired product.

후처리

  1. customThe H2-consumption
  2. filtrationAfter filtration and concentration of the thus-obtained solution
  3. distillationthe residue was distilled at 50°/0.7 hPa

출처 및 근거

ORD 기록
ord-071cb5a54c664502af8d9fd83f1f54ec
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06177400B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트