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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873408Generated: October 31, 2026

Hydrochloric Acid → HCID 59456310, compound

https://huagongshe.com/reaction/1873408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant[5-(4-Ethoxy-2,3-difluorophenyl)selenophen-2-yl]methanolHCID 59456265—
SolventWaterHCID 962—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59456310HCID 59456310—

Reaction Steps

400 mg (10.0 mmol) of sodium hydride (60% suspension in paraffin oil) are washed with n-pentane and suspended in 5 ml of THF. A solution of 1.9 g (about 6.0 mmol) of crude [5-(4-ethoxy-2,3-difluorophenyl)selenophen-2-yl]methanol in 20 ml of THF is added dropwise, and the mixture is stirred for 2 h. 1.0 ml (16.1 mmol) of methyl iodide is metered in, and the batch is stirred at RT for 2 h. Water is carefully added to the reaction mixture, which is then acidified using 2 N hydrochloric acid. The mixture is extracted with MTBE, and the extract is washed with sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The crude product is purified by column chromatography (SiO2, toluene). The further purification is carried out by recrystallisation from ethanol and MTBE. 2-(4-Ethoxy-2,3-difluorophenyl)-5-methoxymethylselenophene is obtained as a solid having an m.p. of 84° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-ba8b38698f844f7899bd3fff4a12e904
Source noteuspto-grants-2012_11