Glycine → Phenylpropionylglycine
Reaction equation
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].[C:6](Cl)(=[O:15])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[OH-].[Na+]>O.CCOCC>[C:9]1([CH2:8][CH2:7][C:6]([NH:1][CH2:2][C:3]([OH:5])=[O:4])=[O:15])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Glycine (1.5 g, 20 mmol) and hydrocinnamoyl chloride (3.37 g, 22 mmol) were reacted in the presence of NaOH (40 mmol) in a mixture of water and ether using the method described in Example 5 Part A. The crude product was extracted into chloroform, dried (MgSO4) and freed of solvent in vacuo leaving a near white solid (3.53 g, 85%). This was recrystallized from EtOAc (13 ml) to give title compound (2.66 g, 64%) m.p. 112°-114° C.
Workup
- extractionThe crude product was extracted into chloroform
- dry with materialdried (MgSO4)
Sources & evidence
- ORD record
- ord-355dc0424a974a6c917e24f6fc746c05
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04734425
Reaction notes
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