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

Aluminium lithium hydride → HCID 69907451, 화합물

HRID 1582686
노트
인쇄 미리보기

반응식

HRID 1582686 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH:7]1([C:15]2[CH:20]=[CH:19][C:18]([C:21]([CH3:28])=[CH:22][C:23](OCC)=[O:24])=[CH:17][CH:16]=2)[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1>CCOCC>[CH:7]1([C:15]2[CH:16]=[CH:17][C:18]([C:21]([CH3:28])=[CH:22][CH2:23][OH:24])=[CH:19][CH:20]=2)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 69906260HCID 69906260, 화합물

생성물 1

HCID 69907451HCID 69907451, 화합물수율 79.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

반응 조건

온도
0 °C

실험 절차

To an ice cooled slurry of LiAlH4 (2.9 g) in dry ether (200 ml) was added a solution of ethyl 3-(4′-cyclooctylphenyl)-but-2-enoate (3d, 10 g) in dry ether (50 ml) dropwise. The reaction mixture was stirred at 0° C. for 2 h. The reaction mixture was quenched with water (11 ml). A solution of 10% NaOH (10 ml) was added and ether layer was decanted. The precipitate was washed with ether and combined extracts were concentrated. The crude product was purified by column chromatography on silica gel to give 6.82 g (79.3% yield) of 3-(4′-cyclooctylphenyl)-2-butenol (4d, formula 4, R=cyclooctyl) m.p. 40-44° C.

후처리

  1. customThe reaction mixture was quenched with water (11 ml)
  2. additionA solution of 10% NaOH (10 ml) was added
  3. customether layer was decanted
  4. washThe precipitate was washed with ether
  5. concentrationwere concentrated
  6. customThe crude product was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-6a1a94bf357b45feb67fde86076f2be9
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06737438B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트