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

Butyl nitrite → HCID 20403190, 화합물

HRID 2164738
노트
인쇄 미리보기

반응식

HRID 2164738 반응식
[CH3:1][C:2]1[N:3]=[C:4]2[C:9]([O:10][CH2:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[N:8][CH:7]=[CH:6][N:5]2[CH:18]=1.[N:19](OCCCC)=[O:20]>O1CCOCC1>[CH3:1][C:2]1[N:3]=[C:4]2[C:9]([O:10][CH2:11][C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[N:8][CH:7]=[CH:6][N:5]2[C:18]=1[N:19]=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10996Butyl nitriteHCID 133890832-Methyl-8-phenylmethoxyimidazo[1,2-a]pyrazine

생성물 1

HCID 20403190HCID 20403190, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 14.2 g 2-methyl-8-phenylmethoxyimidazo[1,2-a]pyrazine, 129.3 g n-butyl nitrite and 142 ml p-dioxane was heated under reflux for 0.5 hr. and decanted from a small amount of gum. The supernatant solution was stirred under vacuum (40°/0.1 mm) and the residue azeotroped with cyclohexane to give 2-methyl-3-nitroso-8-phenylmethoxyimidazo[1,2-a]pyrazine as a soft, green solid which was identified by pmr and ms and immediately reduced (as in Example 6) without further purification.

후처리

  1. temperatureunder reflux for 0.5 hr
  2. customand decanted from a small amount of gum
  3. customthe residue azeotroped with cyclohexane

출처 및 근거

ORD 기록
ord-374f1a7fbbb746f68fe7cd62e25a58d2
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04507294

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트