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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648793Generated: October 31, 2026

Triethylamine → 9-Anthracenylmethyl acrylate

https://huagongshe.com/reaction/1648793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactant9-AnthracenemethanolHCID 73848—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product9-Anthracenylmethyl acrylateHCID 4065231—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 9-hydroxymethylanthracene (20.8 g, 0.1 mol) and triethylamine (11.1 g, 0.11 mol), containing 0.05 g of 2,6-di-tert.butyl-p-cresol, in 200 ml of freshly distilled diethyl ether was cooled with stirring to 0° C., and the temperature of the mixture was kept at about this level while acryloyl chloride (9.32 g, 0.103 mol) was added. The mixture was then warmed to refluxing temperature and heated to reflux for 2 hours. After the mixture had been cooled, 200 ml. of water was added, and the two layers were separated. The organic layer was washed twice with 50 ml portions of cold 10% sulphuric acid and then with a saturated aqueous solution of sodium bicarbonate, while the aqueous acid layer was extracted further with dichloromethane, and the organic layer was washed with a saturated aqueous solution of sodium bicarbonate. Finally, the two organic solutions were mixed, dried over anhydrous magnesium sulphate, and the solvents distilled off. There remained 11.1 g of the title compound as a yellow, semicrystalline oil. It solidified on standing and then had m.pt. 120°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04413052
Source datasetuspto-grants-1983_11
ORD IDord-56fbcc101ce0449480c197c92a95045c
Source noteuspto-grants-1983_11