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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248257Generated: October 26, 2026

Triethylamine → Bis(allyloxycarbonylmethyl) tetrabromoterephthalate

https://huagongshe.com/reaction/1248257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAllyl chloroacetateHCID 76206—
ReactantTetrabromoterephthalic AcidHCID 224162—
SolventChloroformHCID 6212—
ProductBis(allyloxycarbonylmethyl) tetrabromoterephthalateHCID 54532742—

Reaction Steps

To a liquid mixture consisting of 24 parts of tetrabromoterephthalic acid and 60 parts of chloroform, were dropped with stirring 20 parts of allyl chloroacetate. Thereafter, 13 parts of triethylamine were added dropwise while cooling the resulting mixture at 15°-20° C. The mixture was heated until chloroform started to reflux. At the same temperature, the mixture was maintained for 8 hours. After allowing the liquid reaction mixture to cool, it was poured in a separation funnel and washed first with dilute hydrochloric acid and then with water. The organic layer was concentrated under reduced pressures and the resulting white solid was recrystallized from ethyl acetate, thereby obtaining 25 parts of bis(allyloxycarbonylmethyl) tetrabromoterephthalate (hereinafter called "Compound E") as white irregular crystals. (m.p. 146°-148° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522993
Source datasetuspto-grants-1985_06
ORD IDord-e64a6339c34e4bd09301f41f64549772
Source noteuspto-grants-1985_06