Hydrogen Bromide → (-)-alpha-Amino-3-(bromomethyl)-4-hydroxybenzeneacetic acid hydrobromide

HRID 2049209Notes

Reaction equation

HRID 2049209 reaction equation
[NH2:1][CH:2]([C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=1)[C:3]([OH:5])=[O:4].[BrH:13].[CH2:14]=O>>[BrH:13].[NH2:1][CH:2]([C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[C:8]([CH2:14][Br:13])[CH:7]=1)[C:3]([OH:5])=[O:4]

Participants

4

Procedure

To a solution of (-)-α-amino-4-hydroxybenzeneacetic acid (0.6 mole) in a minimum amount of concentrated hydrobromic acid at 35°-40° C. is added 50 ml of aqueous formaldehyde (35-37%) (0.6 mole). The addition of hydrogen bromide gas is begun. After 5-10 minutes, a solid begins to precipitate. Stirring is continued for 30 minutes. The title compound is collected and washed with ether and acetone.

Workup

  1. customto precipitate
  2. waitis continued for 30 minutes
  3. customThe title compound is collected
  4. washwashed with ether and acetone

Sources & evidence

ORD record
ord-fa377f79406d40728fbafab9c9cba44d
Source dataset
uspto-grants-1980_04
Patent number
US04197240

Reaction notes

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