Diethylamine → Bis-(2-hydroxy-3-diethylaminopropyl)terephthalate
Reaction equation
[C:1]([O:16][CH2:17][CH:18]1[O:20][CH2:19]1)(=[O:15])[C:2]1[CH:14]=[CH:13][C:5]([C:6]([O:8][CH2:9][CH:10]2[O:12][CH2:11]2)=[O:7])=[CH:4][CH:3]=1.[CH2:21]([NH:23][CH2:24][CH3:25])[CH3:22]>COCCOC>[OH:12][CH:10]([CH2:11][N:23]([CH2:24][CH3:25])[CH2:21][CH3:22])[CH2:9][O:8][C:6](=[O:7])[C:5]1[CH:4]=[CH:3][C:2]([C:1]([O:16][CH2:17][CH:18]([OH:20])[CH2:19][N:23]([CH2:24][CH3:25])[CH2:21][CH3:22])=[O:15])=[CH:14][CH:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
Diglycidyl terephthalate (145 parts, 1.0 epoxy equivalent) was dissolved in 1,2-dimethoxyethane (145 parts). Diethyl amine (73 parts, 1 mol.) was added at room temperature. The mixture was heated at 60° C. for 20 hours and part of the solvent (75 parts) was stripped off in vacuo. The product, a light-brown viscous solution, had a solids content of 4.45 meq./g theory: 4.59). 2-hydroxy-3-diethylaminiopropyl groups per molecule: 2; molecular weight: 436 (calculated).
Sources & evidence
- ORD record
- ord-8ba2dccde3c54a1798f908b91010000e
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04405662
Reaction notes
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