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

Sodium Hydroxide → 2-Amino-4-bromobenzonitrile

HRID 968571
노트
인쇄 미리보기

반응식

HRID 968571 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([N+:10]([O-])=O)[CH:3]=1.[OH-].[Na+]>Cl>[NH2:10][C:4]1[CH:3]=[C:2]([Br:1])[CH:9]=[CH:8][C:5]=1[C:6]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 2925354-Bromo-2-nitrobenzonitrile

생성물 1

HCID 99206362-Amino-4-bromobenzonitrile

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

To a suspension of 4-bromo-2-nitro-benzonitrile (2.60 g, 0.0115 mol) in 12N HCl at 0° C., add SnCl2-2H2O portionwise. As the reaction is stirred vigorously, a white precipitate will form. After 1 h add ice to the reaction vessel followed by 10N NaOH until the solution is basic. Extract the aqueous mixture with ether (2×) and EtOAc (1×) and wash the combined organic layers with brine. Dry the solution (Na2SO4) and remove the solvents under reduced pressure to give 2-amino-4-bromo-benzonitrile as a beige solid.

후처리

  1. customa white precipitate will form
  2. additionAfter 1 h add ice to the reaction vessel
  3. extractionExtract the aqueous mixture with ether (2×) and EtOAc (1×)
  4. washwash the combined organic layers with brine
  5. dry with materialDry the solution (Na2SO4)
  6. customremove the solvents under reduced pressure

출처 및 근거

ORD 기록
ord-7dda7b7f49c8475baa86c98a934738a0
출처 데이터셋
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07304059B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트