Benzenepropanoyl chloride → N-(3-phenylpropionyl)-D,L-alanine Isobutyl Ester

HRID 411458

Reaction equation

HRID 411458 reaction equation
[C:1]1([CH2:7][CH2:8][C:9](Cl)=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[CH2:13]([O:17][C:18](=[O:22])[CH:19]([CH3:21])[NH2:20])[CH:14]([CH3:16])[CH3:15]>>[CH2:13]([O:17][C:18](=[O:22])[CH:19]([CH3:21])[NH:20][C:9](=[O:10])[CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH:14]([CH3:16])[CH3:15]

Participants

3

Reactant 2

HCID 64801Benzenepropanoyl chlorideHCID 862001092-Methylpropyl 2-aminopropanoate hydrochloride

Product 1

HCID 15480461N-(3-phenylpropionyl)-D,L-alanine Isobutyl Ester

Procedure

Following General Procedure BA above and using 3-phenylpropionyl chloride (Aldrich) and D,L-alanine iso-butyl ester hydrochloride (from Example BB above), the title compound was prepared as a solid having a melting point of from 51-54° C. The reaction was monitored by tlc on silica gel and purification was by extraction with Et2O followed by washes with aqueous K2CO3 and aqueous HCl.

Workup

  1. customof from 51-54° C
  2. customThe reaction was monitored by tlc on silica gel and purification
  3. extractionwas by extraction with Et2O

Sources & evidence

ORD record
ord-d67ff70c34c949448ea6b844b7392692
Source dataset
uspto-grants-2003_05
Patent number
US06559141B2

Linked notes

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