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

Diisoamyl ketone → 2,8-Dimethyl-5-nonanol

HRID 1078104
노트
인쇄 미리보기

반응식

HRID 1078104 반응식
[CH3:1][CH:2]([CH2:4][CH2:5][C:6](=[O:12])[CH2:7][CH2:8][CH:9]([CH3:11])[CH3:10])[CH3:3].[BH4-].[Na+]>CO>[CH3:3][CH:2]([CH2:4][CH2:5][CH:6]([OH:12])[CH2:7][CH2:8][CH:9]([CH3:11])[CH3:10])[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 62421Diisoamyl ketoneHCID 4311764Sodium borohydride

생성물 1

HCID 5578512,8-Dimethyl-5-nonanol수율 40.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 5.63 g (33 mmol) of 2,8-dimethylnonan-5-one in 150 ml of methanol was cooled to 0° C. and treated with 0.8 g (21 mmol) of sodium borohydride. After 1 h, the solution was quenched with 1N HCl; diluted with 1:1 hexane/ether; washed sequentially with 1N NaOH, water, and saturated brine; dried over MgSO4 ; and concentrated in vacuo. Flash chromatography using 10% ethyl acetate in hexane gave 2.30 g (40%) of the desired compound (Rf 0.36, 20% ethyl acetate in hexane) as a colorless oil. 1H NMR (CDCl3) δ0.88 (d, J=7 Hz, 6H), 0.89 (d, J=7 Hz, 6H), 1.1-1.6 (m, 10H), 3.56 (m, 1H).

후처리

  1. customthe solution was quenched with 1N HCl
  2. additiondiluted with 1:1 hexane/ether
  3. washwashed sequentially with 1N NaOH, water, and saturated brine
  4. dry with materialdried over MgSO4
  5. concentrationand concentrated in vacuo

출처 및 근거

ORD 기록
ord-03874758a4774b888f45b30d9b5117ab
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05545750

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트