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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652701Generated: October 30, 2026

Triethylborane → HCID 86741582, compound

https://huagongshe.com/reaction/652701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylboraneHCID 7357—
ReactantMaleic AnhydrideHCID 7923—
ReactantN-Methyl-N-vinylacetamideHCID 18530—
ReactantMaleic AcidHCID 444266—
ReactantHCID 53935447HCID 53935447—
Solventtert-Butyl hydroperoxideHCID 6410—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 86741582HCID 86741582—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673508
Source datasetuspto-grants-1987_06
ORD IDord-20dd3c9e996846798f5585a63a58e8ec
Source noteuspto-grants-1987_06