2-Chloro-5-bromoaniline → 1067197-15-2

HRID 70236Notes

Reaction equation

HRID 70236 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:9])=[C:6]([CH:8]=1)[NH2:7].[N:10]([O-])=O.[Na+]>Cl.O>[ClH:9].[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:9])=[C:6]([NH:7][NH2:10])[CH:8]=1

Participants

5

Conditions

Temperature
5 °C

Procedure

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).

Workup

  1. temperaturewas cooled in an ice/salt bath
  2. temperaturewhile maintaining the temperature below 4° C
  3. stirringThe resulting thick suspension was stirred for 2 h at 5° C.
  4. customthe solid was isolated via filtration
  5. customdried
  6. customfurther dried
  7. additionby adding chlorobutane (500 mL)
  8. temperaturerefluxing
  9. temperatureAfter cooling
  10. customthe solid was isolated by filtration

Sources & evidence

ORD record
ord-caa1a57369bf467da206bf747fd6b458
Source dataset
uspto-grants-2014_09
Patent number
US08822521B2

Reaction notes

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