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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867545Generated: November 2, 2026

Ethyl Acetate → HCID 67529065, compound

https://huagongshe.com/reaction/1867545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant2,4-OxazolidinedioneHCID 97389—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67529065HCID 6752906570.3%

Reaction Steps

A solution of 1.50 g (6 mmol) of 4-bromobenzyl bromide and 0.73 g (7.2 mmol) of 1,3-oxazolidine-2,4-dione in 6 ml of tetrahydrofuran is admixed dropwise with a solution of 1.39 g (12 mmol) of 1,1,3,3-tetramethylguanidine in 6 ml of tetrahydrofuran. The mixture is stirred at ambient temperature overnight. 50 ml of ice-cold aqueous hydrochloric acid (1N) and 100 ml of ethyl acetate are added. The organic phase is separated after settling out and washed successively with 25 ml of water and 25 ml of saturated aqueous sodium chloride solution. It is dried over sodium sulphate and the filtrate is concentrated under reduced pressure. The residue is purified by chromatography on silica gel, eluting with an 80/20 mixture of cyclohexane and ethyl acetate. 1.14 g of product are obtained in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-f4dff77316564d93afc5ea399e47e5e4
Source noteuspto-grants-2009_12