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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974704Generated: October 30, 2026

Imidazole → HCID 14538177, compound

https://huagongshe.com/reaction/974704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14538205HCID 14538205—
SolventAcetonitrileHCID 6342—
ProductHCID 14538177HCID 1453817769.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Thionyl chloride (0.2 g) was added to a cooled solution of 1,1,1-trifluoro-2-(4-ethoxyphenyl)-2-hydroxyprop-3-yl 3-phenoxybenzyl sulphide (0.165 g) and imidazole (0.123 g) in acetonitrile (5 cm3), the temperature of the mixture being maintained at 0° C. The reaction mixture was then allowed to warm to the ambient temperature (21° C.) and stirred for 30 minutes, before being added to a saturated aqueous solution of sodium bicarbonate (7 cm3). The product was extracted into diethyl ether (3×15 cm3), and the combined organic layers were dried over anhydrous magnesium sulphate and evaporated under reduced pressure. The residue was purified by chromatography on a silica gel support, eluting with petroleum ether containing 10% by volume diethy ether, to give 1,1,1-trifluoro-2-chloro-2-(4-ethoxyphenyl)prop-3-yl 3-phenoxybenzyl sulphide (0.12 g) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068461
Source datasetuspto-grants-1991_11
ORD IDord-b66f9e92eceb4b7a8c4c07fc49abbf20
Source noteuspto-grants-1991_11