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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429012Generated: October 29, 2026

Ethyl Acetate → HCID 18354140, compound

https://huagongshe.com/reaction/429012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,3-PropanediolHCID 10442—
ReactantBenzene, 1-(chloromethyl)-3(or 4)-ethenyl-HCID 11768772—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18354140HCID 1835414081%

Reaction Steps

Potassium tert-butoxide (23.07 g, 0.206 mol) was added to a stirred solution of 1,3-propanediol (44.92 g, 0.591 mol) in dry tetrahydrofuran (400 ml) under an atmosphere of nitrogen. The reaction mixture was stirred for 15 min then a solution of vinylbenzylchloride (mixture of meta and para isomers) (30.00 g, 0.197 mol) in dry tetrahydrofuran (100 ml) was added dropwise over 30 min. The reaction was heated at reflux overnight then the tetrahydrofuran was removed in vacuo and the residue taken-up in water (400 ml) and diethyl ether (400 ml). The organic phase was washed with water, dried (magnesium sulfate) and concentrated in vacuo to give a liquid. The liquid was purified by column chromatography over silica gel (eluent 3:1:petrol ether/ethyl acetate, then ethyl acetate) to give the title compound (30.59 g, 0.159 mol, 81%) as a straw colored liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316177B1
Source datasetuspto-grants-2001_11
ORD IDord-5f7b816f21354a50b378a439f47b343d
Source noteuspto-grants-2001_11