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

Ethylene Glycol → 3-Fluoro-4-(2-hydroxyethoxy)benzonitrile

HRID 2078427
노트
인쇄 미리보기

반응식

HRID 2078427 반응식
CC(C)([O-])C.[K+].[F:7][C:8]1[CH:9]=[C:10]([CH:13]=[CH:14][C:15]=1F)[C:11]#[N:12].[CH2:17]([OH:20])[CH2:18][OH:19]>>[F:7][C:8]1[CH:9]=[C:10]([CH:13]=[CH:14][C:15]=1[O:19][CH2:18][CH2:17][OH:20])[C:11]#[N:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 174Ethylene GlycolHCID 5872033,4-DifluorobenzonitrileHCID 23665647Potassium tert-butoxide

생성물 1

HCID 436574753-Fluoro-4-(2-hydroxyethoxy)benzonitrile수율 100%

반응 조건

온도
50 °C

실험 절차

To potassium tert-butoxide (19.35 g) was added ethylene glycol (160 mL). The mixture was then heated to 50° C. At 50° C., 3,4-difluorobenzonitrile (20 g) was added and this was washed in with ethylene glycol (40 mL). The combined solution was heated to 80° C., and held at this temperature for two hours, before being cooled to 20° C. over one hour. The reaction mixture was filtered and washed with ethylene glycol (40 mL). To the filtrate was added water (200 mL) and dichloromethane (200 mL). The layers were separated and the organic layer was concentrated in vacuo, to give the sub-title compound as a waxy white solid (26.1 g, 100% yield).

후처리

  1. washthis was washed in with ethylene glycol (40 mL)
  2. temperatureThe combined solution was heated to 80° C.
  3. temperaturebefore being cooled to 20° C. over one hour
  4. filtrationThe reaction mixture was filtered
  5. washwashed with ethylene glycol (40 mL)
  6. additionTo the filtrate was added water (200 mL) and dichloromethane (200 mL)
  7. customThe layers were separated
  8. concentrationthe organic layer was concentrated in vacuo

출처 및 근거

ORD 기록
ord-f69f4b67b47c4aa4a1b4ecb53780308a
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07928225B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트