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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019190Generated: October 25, 2026

Chlorotrimethylsilane → 2-Trimethylsilyloxy-4-(4-(methylthio)phenyl)-3,4-dihydrofuran

https://huagongshe.com/reaction/1019190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantPentaneHCID 8003—
Reactant2(5H)-FuranoneHCID 10341—
Reactant4-BromothioanisoleHCID 66037—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418306HCID 178418306—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product2-Trimethylsilyloxy-4-(4-(methylthio)phenyl)-3,4-dihydrofuranHCID 18400192—

Reaction Steps

To a solution of 3.86 g (19 mmol) of 4-bromothioanisole in 90 mL of Et2O cooled at −78iC, is added 22 mL of 1.7 M solution of t-BuLi in pentane (38 mmol) dropwise. The reaction mixture is stirred for 15 min at −78 iC and 3.8 g of CuI is added and the reaction mixture is allowed to warm to −40 iC over a period of 30 min. A solution of 1.7 g of 2(5H)-furanone in 10 ml of THF is added. After stirring for 1 h, 2 ml of freshly distilled TMSCl is added dropwise. The reaction mixture is then treated with 2 ml of Et3N and 50 ml of sat. NaHCO3, and extracted with 100 ml of ether. The ether layer is dried over Na2SO4 and concentrated to the crude title compound which is used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486194B2
Source datasetuspto-grants-2002_11
ORD IDord-44129519bb2a4d66accb27ce52159452
Source noteuspto-grants-2002_11