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

4-Bromoaniline → 1-((4-Bromophenyl)diazenyl)pyrrolidine

HRID 522665
노트
인쇄 미리보기

반응식

HRID 522665 반응식
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[N:9]([O-])=O.[Na+].[NH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1>Cl.O.[OH-].[K+]>[Br:1][C:2]1[CH:8]=[CH:7][C:5]([N:6]=[N:9][N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 78074-BromoanilineHCID 31268PyrrolidineHCID 23668193Sodium Nitrite

생성물 1

HCID 3903941-((4-Bromophenyl)diazenyl)pyrrolidine수율 60%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 962Water용매
HCID 14797
Potassium Hydroxide
용매

반응 조건

온도
0 °C

실험 절차

To a solution of 4-bromoaniline (1.7 g, 9.88 mmol) in conc. HCl (2 mL) was added a solution of NaNO2 (682 mg, 9.88 mmol) in water (3 mL) at 0° C. The solution was stirred at 0° C. for 10 minutes, followed by the addition of pyrrolidine (844 mg, 11.86 mmol) in KOH solution (1 mL, 1 N). The resultant mixture was stirred at 0° C. for 0.5 h. The formed precipitate was collected by filtration, washed with 1 mL of ethanol and dried to give the title compound as a yellow solid (1.5 g, yield 60%). MS (ES+) C10H12BrN3 requires: 253, 255, found 254, 256 [M+H]+, purity: 93%.

후처리

  1. filtrationThe formed precipitate was collected by filtration
  2. washwashed with 1 mL of ethanol
  3. customdried

출처 및 근거

ORD 기록
ord-064cb2035ef646a2bdf793158a04c4c1
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334263B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트