1,3-Dibromo-5,5-dimethylhydantoin → 2-Bromo-3,4,5-trimethoxybenzoic acid

HRID 6465

Reaction equation

HRID 6465 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:14][CH3:15])[C:11]=1[O:12][CH3:13])[C:6]([OH:8])=[O:7].CC1(C)N([Br:24])C(=O)N(Br)C1=O>>[Br:24][C:9]1[C:10]([O:14][CH3:15])=[C:11]([O:12][CH3:13])[C:3]([O:2][CH3:1])=[CH:4][C:5]=1[C:6]([OH:8])=[O:7]

Participants

3

Reactant 2

HCID 64791,3-Dibromo-5,5-dimethylhydantoinHCID 83573,4,5-Trimethoxybenzoic Acid

Product 1

HCID 3130972-Bromo-3,4,5-trimethoxybenzoic acid

Procedure

Using the procedure described herein above in Example 1, Method E, 3,4,5-trimethoxybenzoic acid was brominated with DBDMH to provide the following results (assay yields) after reacting for 25 hours at 20°-25° C.:

Workup

  1. customto provide the
  2. customfollowing results
  3. custom(assay yields)

Sources & evidence

ORD record
ord-4d1ae81964184c9cac35555f802dc7dc
Source dataset
uspto-grants-1993_09
Patent number
US05248817

Linked notes

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