Triethylborane → HCID 86741582, compound
Reaction equation
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.C(O)(=O)/C=C\C(O)=O.CC=CNC(=O)C.[CH3:23][N:24]([CH:28]=[CH2:29])[C:25](=[O:27])[CH3:26].C(B(CC)CC)C>O1CCCC1.C(OO)(C)(C)C.CCCCCC>[CH3:23][N:24]([CH:28]=[CH2:29])[C:25](=[O:27])[CH3:26].[C:4]1(=[O:5])[O:6][C:1](=[O:7])[CH:2]=[CH:3]1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 3
Procedure
Copoly(N-methyl-N-vinylacetamide/maleic anhydride) was prepared as follows. About 5 g of maleic anhydride free of maleic acid was dissolved in about 32 g of tetrahydrofuran. This solution was placed in a flask fitted with a dropping funnel, mechanical stirrer and nitrogen inlet. The dropping funnel was charged with about 4 g of N-methylvinylacetamide dissolved in about 13 g of tetrahydrofuran and 0.25 ml of 90% t-butyl hydroperoxide. The temperature of the reaction was adjusted to about 30° C., and the N-methyl-N-vinylacetamide solution was added dropwise over a period of about 4 hours. About 0.5 ml of a 1 Molar solution of triethylborane in hexane was added to the reaction flask at the beginning of the reaction run, and every hour thereafter. At the end of about 7 hours reaction time, the product polymer was precipitated by addition of about 50 ml of petroleum ether. Ths slurry was filtered and washed with diethylether and dried.
Workup
- customThis solution was placed in a flask
- customfitted with a dropping funnel, mechanical stirrer and nitrogen inlet
- customwas adjusted to about 30° C.
- customAt the end of about 7 hours reaction time
- customthe product polymer was precipitated by addition of about 50 ml of petroleum ether
- filtrationThs slurry was filtered
- washwashed with diethylether
- customdried
Sources & evidence
- ORD record
- ord-20dd3c9e996846798f5585a63a58e8ec
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04673508
Reaction notes
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