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

3-Bromobenzonitrile → HCID 178419385, 화합물

HRID 384311
노트
인쇄 미리보기

반응식

HRID 384311 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[C:5]#[N:6].[Cl-].[NH4+].[N-:12]=[N+:13]=[N-:14].[Na+]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]([C:5]2[NH:14][N:13]=[N:12][N:6]=2)[CH:7]=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 233813-BromobenzonitrileHCID 25517Ammonium ChlorideHCID 33557Sodium Azide

생성물 1

HCID 178419385HCID 178419385, 화합물수율 102.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

3-Bromo-benzonitrile 8a (18.2 g, 0.1 mol) and ammonium chloride (5.9 g, 0.11 mol) were dissolved in 80 mL of N,N′-dimethylformamide followed by addition of sodium azide (7.16 g, 0.11 mol) under argon atmosphere. The reaction mixture was heated to 100° C. and reacted overnight. Then the mixture was cooled to 60° C. and concentrated under reduced pressure to remove N,N′-dimethylformamide. The residue was diluted with 100 mL of water and 4 mL of concentrated hydrochloric acid and stirred for 1 hour. The mixture was filtered and dried to obtain the title compound 5-(3-bromo-phenyl)-1H-tetrazole 8b (23 g) as a white solid.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customreacted overnight
  2. temperatureThen the mixture was cooled to 60° C.
  3. concentrationconcentrated under reduced pressure
  4. customto remove N,N′-dimethylformamide
  5. additionThe residue was diluted with 100 mL of water and 4 mL of concentrated hydrochloric acid
  6. filtrationThe mixture was filtered
  7. customdried

출처 및 근거

ORD 기록
ord-c224e77c778e4859bf1839c2dbeacfa8
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367710B2

반응 노트

불러오는 중…