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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873320Generated: November 2, 2026

Hydrochloric Acid → 7,8-Difluoro-3-trimethylsilanylnaphthalen-2-ol

https://huagongshe.com/reaction/1873320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant(2,3-Difluorophenyl)acetyl chlorideHCID 25110985—
SolventDichloromethaneHCID 6344—
Product7,8-Difluoro-3-trimethylsilanylnaphthalen-2-olHCID 58151937—

Reaction Steps

A solution of 50.0 g (0.26 mol) of 2,3-difluorophenylacetyl chloride in 100 ml of dichloromethane is slowly added to a suspension of 71.5 g (0.53 mol) of aluminium(III) chloride in 300 ml of dichloromethane at −20° C. After 30 min at this temperature, trimethylsilylacetylene is metered in, and the mixture is stirred for 30 min. The batch is added to ice-water and acidified using hydrochloric acid. The organic phase is separated off, and the aqueous phase is extracted with ethyl acetate. The combined organic phases are washed successively with sat. sodium hydrogencarbonate soln. and sat. sodium chloride soln. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:ethyl acetate=9:1), giving 7,8-difluoro-3-trimethylsilanylnaphthalen-2-ol as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08303844B2
Source datasetuspto-grants-2012_11
ORD IDord-8b64526dadaa44299e7f2fcf7c9ca7ba
Source noteuspto-grants-2012_11