Benzaldehyde → HCID 53942189, compound

HRID 1655744Notes

Reaction equation

HRID 1655744 reaction equation
O.[NH2:2][C@@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5](=[O:7])[NH2:6].[CH:11](=O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[BH4-].[Na+]>[OH-].[Na+]>[CH2:11]([NH:2][C@@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5](=[O:7])[NH2:6])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Participants

5

Procedure

1.5 g (10 mmol) of D-asparagine hydrate in 5 ml of 2N sodium hydroxide solution were treated with 1.01 ml (10 mmol) of benzaldehyde and the reaction mixture was stirred homogeneously at room temperature for 20 minutes. Subsequently, 114 mg (3 mmol) of sodium borohydride were added portionwise, the mixture was stirred at room temperature for 30 minutes, a further 114 mg of sodium borohydride were added and, finally, the mixture was stirred at room temperature for a further 30 minutes. Thereafter, the aqueous phase was washed with methylene chloride and then adjusted to pH 6-7 with 1N hydrochloric acid, upon which crystallization occurred. The separated crystals were filtered off, washed with water and ether and finally dried in a high vacuum, to obtain 0.6 g (27%) of N-benzyl-3-carbamoyl-D-alanine as a white powder. MS 223 (M+H)+.

Workup

  1. stirringthe mixture was stirred at room temperature for 30 minutes
  2. stirringfinally, the mixture was stirred at room temperature for a further 30 minutes
  3. washThereafter, the aqueous phase was washed with methylene chloride
  4. customadjusted to pH 6-7 with 1N hydrochloric acid, upon which crystallization
  5. filtrationThe separated crystals were filtered off
  6. washwashed with water and ether
  7. customfinally dried in a high vacuum

Sources & evidence

ORD record
ord-82e3d9f00a3542eca5e16a3e4ffa7558
Source dataset
uspto-grants-1993_10
Patent number
US05250517

Reaction notes

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