反应 #1583824

ord-eadaa1ad82b84de1818d0a998748f6e7

反应方程式

Nc1cc(Br)ccc1Cl
5-bromo-2-chloroaniline
O=N[O-].[Na+]
sodium nitrite
Cl.NNc1cc(Br)ccc1Cl
title compound
Cl.NNc1cc(Br)ccc1Cl
5-bromo-2-chlorophenylhydrazine hydrochloride

反应条件

温度
5°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was cooled in an ice/salt bath
  2. 2
    温度while maintaining the temperature below 4° C
  3. 3
    workup.STIRRINGThe resulting thick suspension was stirred for 2 h at 5° C.
  4. 4
    其他the solid was isolated via filtration
  5. 5
    其他dried
  6. 6
    其他further dried
  7. 7
    workup.ADDITIONby adding chlorobutane (500 mL)
  8. 8
    温度refluxing
  9. 9
    温度After cooling
  10. 10
    其他the solid was isolated by filtration

实验过程

A suspension of 5-bromo-2-chloroaniline (23 g, 0.11 mol) in concentrated hydrochloric acid (150 mL) and water (90 mL) was cooled in an ice/salt bath. A solution of sodium nitrite (8 g, 0.11 mol) in water (50 mL) was added dropwise to the reaction mixture while maintaining the temperature below 4° C. After stirring for 30 minutes the suspension was transferred via cannula to a solution of SnCl2 dihydrate in concentrated hydrochloric acid (170 mL) and cooled to 5° C. The resulting thick suspension was stirred for 2 h at 5° C. and the solid was isolated via filtration. The solid was air dried and then further dried by adding chlorobutane (500 mL) and refluxing using a Dean-Stark condenser. After cooling, the solid was isolated by filtration to afford the title compound as an off-white solid (35.3 g). 1H NMR (CD3COCD3): δ 10.25 (br s, 1H), 8.32 (br s, 2H) 7.38 (d, 1H), 7.30 (d, 1H), 7.16 (dd, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09198433B2uspto-grants-2015_12