Lactide, L- → HCID 131729080, compound
Reaction equation
C[C@@H:2]1[O:9]C(=O)[C@H](C)[O:5][C:3]1=[O:4].[CH2:11]([O:18][C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][CH:26]1[C:31](=[O:32])[O:30]CC(=O)[NH:27]1)=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH3:34][C@@H:35]1[O:42]C(=O)[C@H](C)[O:38][C:36]1=[O:37].C(OC(NCCCCC1C(=O)OCC(=O)N1)=O)C1C=CC=CC=1>C(Cl)(Cl)Cl>[C:3]([OH:5])(=[O:4])[CH2:2][OH:9].[CH2:11]([O:18][C:19]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][C@@H:26]([C:31]([OH:32])=[O:30])[NH2:27])=[O:20])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1.[C:36]([OH:38])(=[O:37])[C@H:35]([CH3:34])[OH:42]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
According to the molar ratio of L-Lactide/3-[4-(benzyloxycarbonylamino) butyl]-morpholine-2,5-dione monomer-=1: 9, 40.5 g L-Lactide and 10 g 3-[4-(benzyloxycarbonylamino) butyl]-morpholine-2,5-dione monomer are weighed and put into ampule. Then 5 ml stannous octoate chloroform solution of 30 mg/ml is injected. After volatilization of the chloroform under vacuum, the ampule is sealed with alcohol blast burner. Finally, the sealed ampule is put into oil-bath of 90-140° C. for 12-72 h to obtain poly (glycolic acid-Nε-benzyloxycarbonyl-L-lysine-L-lactic acid).
Sources & evidence
- ORD record
- ord-71fc0ce0a3104cf2b9a24bfe063e3e84
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989532B2
Reaction notes
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