Sodium borohydride → tert-Butyl (3-hydroxypropyl)methylcarbamate

HRID 1649904Notes

Reaction equation

HRID 1649904 reaction equation
C[O:2][C:3](=O)[CH2:4][CH2:5][N:6]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[CH3:7].[BH4-].[Na+]>CO.O>[C:11]([O:10][C:8]([N:6]([CH2:5][CH2:4][CH2:3][OH:2])[CH3:7])=[O:9])([CH3:14])([CH3:13])[CH3:12]

Participants

5

Procedure

To a solution of N-t-butoxycarbonyl-N-methyl-β-alanine methyl ester (3.911 g) in methanol (20 ml) and water (20 ml) was added sodium borohydride (6.81 g) portionwise at 4° C. and the mixture was stirred at room temperature for 3 hours. The solution was concentrated in vacuo, and the residue was portioned between ethyl acetate (100 ml) and 0.5N hydrochloric acid (100 ml). The separated organic layer was washed with 0.5N hydrochloric acid (100 ml), water (100 ml), aqueous sodium bicarbonate (100 ml), water (100 ml) and brine (100 ml) successively,and dried over magnesium sulfate. Evaporation of the solvent gave 3-(N-t-butoxycarbonyl-N-methylamino)propanol (2.48 g) as an oil.

Workup

  1. concentrationThe solution was concentrated in vacuo
  2. washThe separated organic layer was washed with 0.5N hydrochloric acid (100 ml), water (100 ml), aqueous sodium bicarbonate (100 ml), water (100 ml) and brine (100 ml)
  3. dry with materialsuccessively,and dried over magnesium sulfate
  4. customEvaporation of the solvent

Sources & evidence

ORD record
ord-7fc11ee7941d4a939de8b24d15e53636
Source dataset
uspto-grants-1990_05
Patent number
US04921855

Reaction notes

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