Ammonia → 135205-37-7

HRID 1729321Notes

Reaction equation

HRID 1729321 reaction equation
[C:1]([O:5][CH:6]1[O:9][CH:7]1[CH3:8])([CH3:4])([CH3:3])[CH3:2].[NH3:10]>>[NH2:10][CH2:8][CH:7]([OH:9])[CH2:6][O:5][C:1]([CH3:4])([CH3:3])[CH3:2]

Participants

3

Procedure

100 g of 1,2-epoxypropyl tert.-butyl ether are added dropwise to 500 ml of conc. aqueous ammonia under ice-cooling and tile mixture is stirred at room temperature for 20 hours. The reaction mixture is evaporated under reduced pressure to remove the aqueous ammonia. Chloroform is added to the residue. The mixture is dried with potassium carbonate. Insoluble materials are filtered off and the filtrate is evaporated to remove the solvent. The residue is distilled under reduced pressure. 49.3 g of 1-amino-3-tert.-butoxy-2-propanol are obtained.

Workup

  1. temperaturecooling
  2. customThe reaction mixture is evaporated under reduced pressure
  3. customto remove the aqueous ammonia
  4. additionChloroform is added to the residue
  5. dry with materialThe mixture is dried with potassium carbonate
  6. filtrationInsoluble materials are filtered off
  7. customthe filtrate is evaporated
  8. customto remove the solvent
  9. distillationThe residue is distilled under reduced pressure

Sources & evidence

ORD record
ord-a4996401a11e44da9e3c34a1e3b007d3
Source dataset
uspto-grants-1994_07
Patent number
US05332754

Reaction notes

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