Hydrochloric Acid → HCID 67571971, compound

HRID 1734625Notes

Reaction equation

HRID 1734625 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5](C=O)=[CH:4][C:3]=1[OH:11].[OH-:12].[Na+].OO.Cl>>[Br:1][C:2]1([OH:12])[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][CH:3]1[OH:11]

Participants

5

Procedure

A stirred solution of 25.0 grams (0.106 mole) of 2-bromo-4-chloro-5-formylphenol in 106 mL (0.106 mole) of aqueous 1N sodium hydroxide was warmed to about 50° C., and 150 mL (0.133 mole) of aqueous 3% hydrogen peroxide was added dropwise. Upon completion of addition, the reaction mixture was allowed to cool to ambient temperature as it stirred for about 18 hours. After this time, the reaction mixture was made acidic with aqueous 6N hydrochloric acid. The mixture was then filtered to collect a solid. The solid was washed with water and dried under vacuum, yielding 21.2 grams of 2-bromo-4-chlorocatechol. The NMR spectrum was consistent with the proposed structure.

Workup

  1. additionUpon completion of addition
  2. filtrationThe mixture was then filtered
  3. customto collect a solid
  4. washThe solid was washed with water
  5. customdried under vacuum

Sources & evidence

ORD record
ord-5980b7dcb7e7433e8704fe9b6d678e39
Source dataset
uspto-grants-1996_07
Patent number
US05534518

Reaction notes

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