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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34609Generated: October 30, 2026

Diethyl Ether → 4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcohol

https://huagongshe.com/reaction/34609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl AcetateHCID 8857—
Reactant2-[4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyloxy]-tetrahydropyranHCID 13911481—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product4-Trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcoholHCID 13911482—

Reaction Conditions

Temperature25 °C

Reaction Steps

The crude tetrahydropyranyl ether prepared in Stage (i) was dissolved in methanol (20 cm3), and to the stirred solution was added concentrated hydrochloric acid (3 drops). After stirring for 16 hours at the ambient temperature (ca. 25° C.), the reaction mixture was poured into ethyl acetate, washed with water and brine, and dried. Evaporation of the solvent under reduced pressure gave a yellow oil which was subjected to column chromatography on silica gel using petroleum ether (boiling range 40°-60° C.) containing diethyl ether (10% gradually increased to 40% by volume) as eluent to give 4-trimethylsilyl-2,3,5,6-tetrafluorobenzyl alcohol (0.79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762835
Source datasetuspto-grants-1988_08
ORD IDord-c63bc3ba6643468999e4739e9fb348d1
Source noteuspto-grants-1988_08