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

1-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-one → HCID 20569421, 화합물

HRID 746366
노트
인쇄 미리보기

반응식

HRID 746366 반응식
[CH3:1][C:2]([C:4]1[CH2:9][C:8]([CH3:11])([CH3:10])[CH2:7][CH2:6][CH:5]=1)=[O:3].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[CH3:1][CH:2]([OH:3])[C:4]1[CH2:9][C:8]([CH3:11])([CH3:10])[CH2:7][CH2:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 126685191-(5,5-Dimethylcyclohex-1-en-1-yl)ethan-1-oneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 20569421HCID 20569421, 화합물수율 85%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanone (13.1 g, 85.8 mmol) in Et2O (50 ml) was added dropwise with stirring within 50 min. to a suspension of LAH (895 mg, 23.6 mmol) in Et2O (150 ml). The reaction mixture was refluxed for 1 h prior to quenching at 0° C. by careful addition of water (50 ml) followed by 5 N aq. HCl (50 ml). The organic layer was separated and the aqueous one extracted with Et2O. The combined ethereal solutions were washed with water and brine, dried (Na2SO4), and concentrated in a rotary evaporator. Silica-gel FC (pentane/Et2O, 9:1, Rf=0.14) of the resulting residue (14.7 g) gave 11.2 g (85%) of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanol.

후처리

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. customto quenching at 0° C. by careful addition of water (50 ml)
  3. customThe organic layer was separated
  4. extractionthe aqueous one extracted with Et2O
  5. washThe combined ethereal solutions were washed with water and brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated in a rotary evaporator

출처 및 근거

ORD 기록
ord-aaf271fcf2e345e0aff63f8e9b08bf0c
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07393822B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트