Dicyclohexylcarbodiimide → Benzyl N-(2-benzylacryloyl)glycinate
Reaction equation
[CH2:1]([C:8](=[CH2:12])[C:9]([OH:11])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:13]([O:20][C:21](=[O:24])[CH2:22][NH2:23])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C1C=CC2N(O)N=NC=2C=1.C1CCC(N=C=NC2CCCCC2)CC1>C1COCC1.C(Cl)(Cl)Cl.C(N(CC)CC)C>[CH2:13]([O:20][C:21](=[O:24])[CH2:22][NH:23][C:9](=[O:11])[C:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[CH2:12])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
2.42 g (15 mmoles) of 2-benzyl acrylic acid are dissolved in 30 ml of THF and 10 ml of CHCl3. There is added a solution in 50 ml of THF of 1.87 g of glycine benzyl ester hydrochlorate, 2.2 g of triethylamine, then 2.20 g of HOBT and 3.4 g of DCC. The mixture is stirred for 20 hours at room temperature. The precipitate of DCU formed is collected. After evaporating to dryness and taking up with ethyl acetate the organic phase is washed in succession with 2×20 ml of citric acid, then 3×20 ml of NaHCO3. The material is concentrated under a vacuum and the rest of the DCU formed is suction filtered. A yellow oil which crystallizes slowly is obtained.
Workup
- customThe precipitate of DCU formed
- customis collected
- customAfter evaporating to dryness
- washis washed in succession with 2×20 ml of citric acid
- concentrationThe material is concentrated under a vacuum
- customthe rest of the DCU formed
- filtrationfiltered
- customA yellow oil which crystallizes slowly
- customis obtained
Sources & evidence
- ORD record
- ord-fb5cebb86ea943ea8f92947cad6a839e
- Source dataset
- uspto-grants-1988_04
- Patent number
- US04738803
Reaction notes
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