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

Water → 2-Oxo-1-(2-propen-1-yl)-1,2-dihydro-7-quinolinecarbonitrile

HRID 656890
노트
인쇄 미리보기

반응식

HRID 656890 반응식
[I-].[C:2]([C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[CH:9][CH:10]=[N+:11]2[CH2:14][CH:15]=[CH2:16])=[CH:6][CH:5]=1)#[N:3].[OH-:17].[K+].O>O1CCOCC1.O.[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+]>[O:17]=[C:10]1[CH:9]=[CH:8][C:7]2[C:12](=[CH:13][C:4]([C:2]#[N:3])=[CH:5][CH:6]=2)[N:11]1[CH2:14][CH:15]=[CH2:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 14797Potassium HydroxideHCID 68993985HCID 68993985, 화합물

생성물 1

HCID 689923622-Oxo-1-(2-propen-1-yl)-1,2-dihydro-7-quinolinecarbonitrile수율 55%

시약·촉매·용매 2

HCID 178511488HCID 178511488, 화합물촉매HCID 21886435
1,4-Dioxane--water (1/1)
용매

실험 절차

A mixture of 7-cyano-1-(2-propen-1-yl)quinolinium iodide (1.75 g, 5.4 mmol), potassium hydroxide (1.33 g, 23.76 mmol) and potassium ferricyanide (3.9 g, 11.9 mmol) in 50% 1,4-dioxane/water was stirred at rt for 2 h. Water (50 ml) was then added and the organic phase was extracted with 10% methanol/DCM (2×100 ml). The combined organic phases were washed with water (100 ml) then dried and evaporated. The residue was chromatographed on silica gel, eluting with 0-5% methanol-DCM to afford the desired compound (0.6 g, 55%).

후처리

  1. extractionthe organic phase was extracted with 10% methanol/DCM (2×100 ml)
  2. washThe combined organic phases were washed with water (100 ml)
  3. customthen dried
  4. customevaporated
  5. customThe residue was chromatographed on silica gel
  6. washeluting with 0-5% methanol-DCM

출처 및 근거

ORD 기록
ord-32c50c7e857a4d43916ba48d4e400688
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071592B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트