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

Acetone → 3-Octen-2-one

HRID 464103
노트
인쇄 미리보기

반응식

HRID 464103 반응식
[Li+].[I-].[CH3:3][C:4]([CH3:6])=[O:5].[CH:7](=O)[CH2:8][CH2:9][CH2:10][CH3:11].O>C(OCC)C>[CH3:3][C:4](=[O:5])/[CH:6]=[CH:7]/[CH2:8][CH2:9][CH2:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 962WaterHCID 8063PentanalHCID 66321Lithium iodide

생성물 1

HCID 53632293-Octen-2-one

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 7.73 g (58 mM) of anhydrous LiI and 1.47 ml (20 mM) of acetone in 35 ml of diethyl ether was heated to gentle reflux. To this solution was added dropwise a solution of 1.59 ml (15.0 mM) 1-pentanal in 5 ml diethyl ether over 10 minutes. The solution was then heated at reflux for 6 hours. After the solution was cooled to ambient temperature water was added and the layers separated. The ether phase was washed once with brine and dried over anhydrous MgSO4. The diethyl ether was removed by distillation at atmospheric pressure followed by distillation of the residue. There was obtained 0.52 g (27%) of a highly mobile colorless liquid. 1H NMR (CDCl3):6.80δ (dt,1H,JHH =7Hz, 16Hz), 6.01δ (d,1H,JHH =16Hz), 2.20δ (s,3H).

후처리

  1. temperatureThe solution was then heated
  2. temperatureat reflux for 6 hours
  3. additionwas added
  4. customthe layers separated
  5. washThe ether phase was washed once with brine
  6. dry with materialdried over anhydrous MgSO4
  7. customThe diethyl ether was removed by distillation at atmospheric pressure
  8. distillationfollowed by distillation of the residue
  9. customThere was obtained 0.52 g (27%) of a highly mobile colorless liquid

출처 및 근거

ORD 기록
ord-4ac4febf14dd4b0893b14d6cdc31cb0a
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04546104

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트