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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362705Generated: November 2, 2026

Sodium hydride → HCID 15381168, compound

https://huagongshe.com/reaction/362705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant(3,4-Dichlorophenyl)acetonitrileHCID 76690—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15381168HCID 1538116871.4%

Reaction Steps

A solution of 50.8 g of 3,4-dichlorophenyl-acetonitrile in 250 ml of THF is added dropwise at a temperature below 20° C. to a suspension of 12 g of sodium hydride (55% dispersion in oil) in 175 ml of THF and the reaction mixture is stirred for 2 hours at RT. It is cooled to -20° C., a solution of 62.5 g of 1-bromo-3-(tetrahydropyran-2-yloxy)propane in 60 ml of THF is added dropwise and the reaction mixture is stirred while the temperature is allowed to rise to RT. It is poured into a solution of 31 g of ammonium chloride in 1.4 liters of water and extracted with ether, the combined organic phases are washed with saturated NaCl solution and dried over MgSO4 and the solvents are evaporated off under vacuum. The residue is chromatographed on silica using toluene and then a toluene/AcOEt mixture (95/5; v/v) as the eluent to give 64 g of the expected product, which is used as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869663
Source datasetuspto-grants-1999_02
ORD IDord-fab633c1b2bb46769240941388ca9de0
Source noteuspto-grants-1999_02