Triethylamine → HCID 12796233, compound
Reaction equation
[N+](C1C=CC(O[C:11](=[O:24])[CH2:12][C:13]2[CH:18]=[CH:17][C:16]([O:19][CH2:20][CH:21]=[CH2:22])=[C:15]([Cl:23])[CH:14]=2)=CC=1)([O-])=O.Cl.[CH3:26][O:27][C:28](=[O:31])[CH2:29][NH2:30].C(N(CC)CC)C>C(Cl)(Cl)Cl>[CH3:26][O:27][C:28](=[O:31])[CH2:29][NH:30][C:11](=[O:24])[CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:20][CH:21]=[CH2:22])=[C:15]([Cl:23])[CH:14]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
4-Allyloxy-3-chloro-phenylacetic acid p-nitrophenyl ester (3.69 g) was dissolved in chloroform (30 ml). To the solution was added glycine methyl ester hydrochloride (1.5 g) in dry chloroform (30 ml) containing dry triethylamine (1.4 ml), and the solution was stirred at 40° C. for 4 hrs.
Sources & evidence
- ORD record
- ord-9603423fb5324a3dadd784efa668de00
- Source dataset
- uspto-grants-1985_03
- Patent number
- US04505898
Reaction notes
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