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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50058Generated: October 25, 2026

Sodium hydride → Ethyl 5-cyano-5-(3,4-dichlorophenyl)pentanoate

https://huagongshe.com/reaction/50058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant(3,4-Dichlorophenyl)acetonitrileHCID 76690—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-cyano-5-(3,4-dichlorophenyl)pentanoateHCID 2274180845.8%

Reaction Steps

11.8 g of a 55% dispersion of sodium hydride in oil are suspended in 100 ml of THF and cooled in an ice bath, a solution of 50 g of 3,4-dichlorophenylaceto-nitrile in 50 ml of THF is added dropwise and the reaction mixture is stirred for 3 hours at RT. It is cooled again in an ice bath, a solution of 52.4 g of ethyl 4-bromobutanoate in 50 ml of THF is added dropwise and the mixture is stirred overnight at RT. It is concentrated under vacuum, the residue is taken up with water and extracted with ether, the organic phase is washed with water, with a buffer solution of pH 2, with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using toluene and then a toluene/AcOEt mixture (100/5; v/v) as the eluent to give 36.9 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710042B2
Source datasetuspto-grants-2004_03
ORD IDord-1a468d6f06e742b598e42836aaab8419
Source noteuspto-grants-2004_03