Hydrochloric Acid → FSCZNKNUJVBMPY-UHFFFAOYSA-N
Reaction equation
C([O:8][C:9](=[O:23])[CH2:10][NH:11][C:12](=[O:22])[C:13]([CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[CH2:14])C1C=CC=CC=1.CO.[OH-].[Na+].Cl>O>[CH2:15]([C:13](=[CH2:14])[C:12]([NH:11][CH2:10][C:9]([OH:23])=[O:8])=[O:22])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
2.10 (6.8 mmoles) of N-(2-benzyl propenoyl-glycine benzyl ester, M.P. =60° C, are stirred at 10° C. for 2 hours with a mixture of 30 ml of methanol and 0.27 g of NaOH (6.8 mmoles), dissolved in 5 ml of water. The pH is brought to 1 by the addition of 2N HCl and the material is extracted with ethyl acetate. The solvent is washed with 2×20 ml of water, dried and evaporated under a vacuum. 1.36 g of crystals are obtained.
Workup
- extractionthe material is extracted with ethyl acetate
- washThe solvent is washed with 2×20 ml of water
- customdried
- customevaporated under a vacuum
Sources & evidence
- ORD record
- ord-f826b4d5a1604ef785a6739d815597e7
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04618708
Reaction notes
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