Hydrochloric Acid → HCID 12842605, compound

HRID 2413658Notes

Reaction equation

HRID 2413658 reaction equation
C([NH:8][C:9]([CH3:15])([CH2:12][CH2:13][OH:14])[CH2:10][OH:11])C1C=CC=CC=1.[ClH:16]>CCO.[Pd]>[ClH:16].[NH2:8][C:9]([CH3:15])([CH2:12][CH2:13][OH:14])[CH2:10][OH:11]

Participants

5

Procedure

2-Benzylamino-2-methyl-1,4-butanediol (36E, 31.08 g, 0.149 mol) was dissolved in 95% EtOH (240 mL) containing conc. HCl (21 mL, 0.25 mol) and 5% Pd/C (10.0 g) and reduced in a Parr apparatus at 40 psi over 37 h at RT. The catalyst was then removed by filtration and the solvent removed by rotary evaporation (bath at 60°) to give 20.91 g of 2-amino-2-methyl-1,4-butanediol hydrochloride (90.2%) as a clear, thick, colorless oil with acceptable NMR and mass spectra. It was used without further purification. This compound has been reported as its acetate salt (G. Cardillo et al., Chem. Commun. 1308, 1982), but no data was given. Attempts to duplicate the latter procedure were unsuccessful.

Workup

  1. customThe catalyst was then removed by filtration
  2. customthe solvent removed by rotary evaporation (bath at 60°)

Sources & evidence

ORD record
ord-e40810913ac34ae68c9102c430f04db1
Source dataset
uspto-grants-1988_01
Patent number
US04719049

Reaction notes

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