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

Methanol → 6-(2-Oxoethyl)nicotinonitrile

HRID 1466046
노트
인쇄 미리보기

반응식

HRID 1466046 반응식
[CH2:1]([C:4]1[N:9]=[CH:8][C:7]([C:10]#[N:11])=[CH:6][CH:5]=1)[CH:2]=C.C[OH:13]>C(Cl)Cl>[O:13]=[CH:2][CH2:1][C:4]1[N:9]=[CH:8][C:7]([C:10]#[N:11])=[CH:6][CH:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 107968686-Allylnicotinonitrile

생성물 1

HCID 895250136-(2-Oxoethyl)nicotinonitrile

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-70 °C

실험 절차

A mixture of 6-(Prop-2-en-1-yl)pyridine-3-carbonitrile (4.8 g, 33 mmol) in 80 mL of DCM and 20 mL of MeOH was cooled to −70° C. Ozone was bubbled through the mixture until the mixture turned blue (about 20 minutes). The excess of ozone was removed by flush with N2 flow until the mixture turned colorless. 5 mL of Me2S was added to the mixture which was then warmed slowly to room temperature and stirred for 2 hours. The solvent was removed under vacuum below 30° C. to afford the title compound which was used without further purification.

후처리

  1. customOzone was bubbled through the mixture until the mixture
  2. custom(about 20 minutes)
  3. customThe excess of ozone was removed
  4. customby flush with N2 flow until the mixture
  5. addition5 mL of Me2S was added to the mixture which
  6. temperaturewas then warmed slowly to room temperature
  7. customThe solvent was removed under vacuum below 30° C.

출처 및 근거

ORD 기록
ord-9a02be7ad62f409aa48c5221d2671734
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999990B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트