Hydrogen Bromide → Benzenepropanol, β-amino-3-hydroxy-, hydrobromide (1:1)
Reaction equation
Cl.Cl.[NH2:3][CH:4]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14]C)[CH:9]=1)[CH2:5][OH:6].[BrH:16]>>[BrH:16].[NH2:3][CH:4]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([OH:14])[CH:9]=1)[CH2:5][OH:6]Participants
4
Procedure
8 gm of the hydrochloride obtained in (a) were admixed with 80 ml of 48% hydrobromic acid, and the mixture was refluxed for one hour. Thereafter, the reaction mixture was evaporated to dryness, the residue was stripped of water by entrainment with xylene, the solvent was distilled off, and the residue was recrystallized from ethyl acetate, yielding 6 gm (66% of theory) of the compound of the formula ##STR9## which had a melting point of 150°-152° C.
Workup
- temperaturethe mixture was refluxed for one hour
- customThereafter, the reaction mixture was evaporated to dryness
- distillationthe solvent was distilled off
- customthe residue was recrystallized from ethyl acetate
- customyielding 6 gm (66% of theory) of the compound of the formula ##STR9## which
Sources & evidence
- ORD record
- ord-c8d6d06b0ba54d4ca0663bb872b83659
- Source dataset
- uspto-grants-1977_11
- Patent number
- US04058642
Reaction notes
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