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

Aluminium lithium hydride → (2-Ethylpyridin-3-yl)methanol

HRID 1685
노트
인쇄 미리보기

반응식

HRID 1685 반응식
[Li+].[CH2:2]([C:4]1[N:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6]([O-])=[O:7])[CH3:3].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:2]([C:4]1[C:5]([CH2:6][OH:7])=[CH:9][CH:10]=[CH:11][N:12]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 1317205572-Ethyl nicotinic acid lithium salt

생성물 1

HCID 19690951(2-Ethylpyridin-3-yl)methanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The 2-ethyl nicotinic acid lithium salt (5 g, 3.18 mmol) in distilled THF (400 mL) under nitrogen was cooled to 0° C. and lithium aluminum hydride (1M in THF) (25 mL) was added dropwise. The reaction was stirred for 3 hours at room temperature then cooled to 0° C. and quenched with EtOAc (949 μL), then H2O (949 μL), then 15% NaOH (949 μL), followed by H2O (2.8 mL). The solution was filtered and the solvent removed under reduced pressure. Toluene was added and the solvent was removed under reduced pressure to give the desired 2-ethyl-3 -hydroxymethylpyridine.

후처리

  1. temperaturethen cooled to 0° C.
  2. customquenched with EtOAc (949 μL)
  3. filtrationThe solution was filtered
  4. customthe solvent removed under reduced pressure
  5. additionToluene was added
  6. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-aaa0ddfbf41e452299afe064a36ec3cd
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05726172

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트