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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742626Generated: October 26, 2026

Ethyl bromoacetate → Ethyl beta-tetrahydropyranyloxyethyl-beta-cyano-beta-(3,4-dichlorophenyl)propionate

https://huagongshe.com/reaction/742626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(3-Cyano-3-(3,4-dichlorophenyl)propyl)oxytetrahydropyranHCID 15670807—
ProductEthyl beta-tetrahydropyranyloxyethyl-beta-cyano-beta-(3,4-dichlorophenyl)propionateHCID 67635049—

Reaction Steps

21 g of the nitrile prepared above according to (a) are dissolved in 100 ml of tetrahydrofuran, a solution of 0.067 mol of lithium diisopropylamide in 100 ml of tetrahydrofuran is then added dropwise at room temperature and the reaction mixture is stirred for one hour at room temperature. 12 g of ethyl bromoacetate are then added and the mixture is heated at 50° C. for two hours. The mixture is cooled, poured into a saturated solution of ammonium chloride and extracted with ethyl ether, the extract is washed with water and the ether phase is separated off by decantation, dried over Na2SO4 and concentrated under vacuum. The residue is purified by chromatography on silica gel using dichloromethane/ethyl acetate (100/1 v/v) as the eluent. Concentration of the pure fractions gives 13 g of the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554763
Source datasetuspto-grants-1996_09
ORD IDord-98d4b20686af47c1999dd75e37492fae
Source noteuspto-grants-1996_09