Triethylamine → HCID 12796234, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=O)=[CH:7][C:6]=1[Cl:15])[CH:2]=[CH2:3].Cl.[CH2:17]([O:19][C:20](=[O:23])[CH2:21][NH2:22])[CH3:18].C(N(CC)CC)C.C1CCC(N=C=NC2CCCCC2)CC1>O1CCCC1.C(Cl)(Cl)Cl>[CH2:17]([O:19][C:20](=[O:23])[CH2:21][NH:22][C:12](=[O:14])[CH2:11][C:8]1[CH:9]=[CH:10][C:5]([O:4][CH2:1][CH:2]=[CH2:3])=[C:6]([Cl:15])[CH:7]=1)[CH3:18]Participants
7
Procedure
4-Allyloxy-3-chloro-phenylacetic acid (4.3 g) was dissolved in dry tetrahydrofuran (20 ml). To the solution was added glycine ethyl ester hydrochloride (2.85 g) in dry chloroform (30 ml) containing dry triethylamine (2.8 ml). DCC (4.1 g) was added and the reaction mixture was stirred overnight at room temperature.
Sources & evidence
- ORD record
- ord-24d1807aa75a4ca9a0e17173b42ba950
- Source dataset
- uspto-grants-1985_03
- Patent number
- US04505898
Reaction notes
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