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

Sodium borohydride → 2,2-Difluoro-2-(pyridin-4-yl)-ethanol

HRID 1615086
노트
인쇄 미리보기

반응식

HRID 1615086 반응식
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([F:14])([F:13])[C:8](OCC)=[O:9])=[CH:3][CH:2]=1.[BH4-].[Na+]>C(O)C>[F:14][C:7]([F:13])([C:4]1[CH:5]=[CH:6][N:1]=[CH:2][CH:3]=1)[CH2:8][OH:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 59633981Ethyl 2,2-difluoro-2-(pyridin-4-yl)acetate2회

생성물 1

HCID 596339072,2-Difluoro-2-(pyridin-4-yl)-ethanol수율 17.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of ethyl pyridin-4-yl-difluoroacetate (0.59 g) prepared in (1) in ethanol (10 mL) was added NaBH4 (0.11 g) at 0° C. The reaction mixture was stirred at RT for 2 hr. The solvent was removed under reduced pressure. Water was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous NaHCO3, and then dried over MgSO4. The solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (Developing solvent: ethyl acetate) to give the title compound (0.082 g, 1%).

후처리

  1. customThe solvent was removed under reduced pressure
  2. additionWater was added to the residue
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated aqueous NaHCO3
  5. dry with materialdried over MgSO4
  6. customThe solvent was removed under reduced pressure
  7. customThe residue was purified by silica gel chromatography (Developing solvent: ethyl acetate)

출처 및 근거

ORD 기록
ord-f6aefafcc0f24584a3a37d4800df952b
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765739B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트