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

Ammonium → HCID 18977005, 화합물

HRID 2393724
노트
인쇄 미리보기

반응식

HRID 2393724 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[N:8]([CH2:11][CH2:12][CH2:13][CH2:14][N:15]=[N+:16]=[N-:17])=[N+:9]=[N-:10].[NH4+:18]>CCCCC.CCCCCC>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:10][N:9]=[N:8][CH2:11][CH2:12][CH2:13][CH2:14][N:15]=[N:16][NH:17][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 223AmmoniumHCID 79732-BromopyridineHCID 136209641,4-Diazidobutane

생성물 1

HCID 18977005HCID 18977005, 화합물

시약·촉매·용매 2

HCID 8003Pentane용매2회HCID 8058Hexane용매

실험 절차

A solution of 3.95 g (25 mmoles) of 2-bromopyridine in 20 ml of dry pentane was added dropwise to 10 ml. of 2.5M butylithium in hexane at -78° C. To the resulting yellow slurry was added dropwise with stirring 1.75 g (12.5 mmoles) of 1,4-diazidobutane in 10 ml. of pentane. Stirring was continued for 2 hr. at -78° and then the reaction mixture was allowed to warm to room temperature. The reaction mixture was treated with 60 ml. of ammonium buffer which caused a precipitate to appear after the reaction was cooled to -78° C. The solid was filtered off. It was poorly soluble in common solvents such as halomethanes, acetone, methanol and water. It was sparingly soluble in dimethylsulfoxide. The yield was 2.3 g., m.p. 133-136. Spectroscopic data were consistent with the structure.

후처리

  1. customat -78° C
  2. additionTo the resulting yellow slurry was added dropwise
  3. customat -78°
  4. additionThe reaction mixture was treated with 60 ml
  5. temperaturewas cooled to -78° C
  6. filtrationThe solid was filtered off

출처 및 근거

ORD 기록
ord-2593938d6c904d25a07ee2dfcc429eb7
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05808038

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트