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N-bromobutanimide → 2-Amino-5-bromo-3-fluorobenzoic acid

HRID 56468
Notes
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Reaction equation

HRID 56468 reaction equation
[NH2:1][C:2]1[C:10]([F:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Br:12]N1C(=O)CCC1=O>ClCCl>[NH2:1][C:2]1[C:10]([F:11])=[CH:9][C:8]([Br:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 67184N-bromobutanimideHCID 5864082-Amino-3-fluorobenzoic acid

Product 1

HCID 404245972-Amino-5-bromo-3-fluorobenzoic acidYield 78%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A solution of 2-amino-3-fluorobenzoic acid (10.85 g, 70 mmol) in dichloromethane (175 mL) was added N-bromosuccinimide (12.46 g, 70 mmol), and the mixture was stirred at room temperature for 2 hours. The precipitate was filtered and washed with dichloromethane (100 mL*3) to give the title compound (12.7 g, 78%) as a grey solid, which was directly used in the next step without further purification. MS (ES+) C7H5BrFNO2 requires: 233, 235, found: 232, 234 [M+H]+.

Workup

  1. filtrationThe precipitate was filtered
  2. washwashed with dichloromethane (100 mL*3)

Sources & evidence

ORD record
ord-b4471c6e3f3b489f9ebd1151cd0d9116
Source dataset
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09434700B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes