Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269265Generated: October 31, 2026

Tetrahydrofuran → 4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisole

https://huagongshe.com/reaction/2269265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-(Trifluoromethyl)dibenzothiophenium trifluoromethanesulfonateHCID 2777507—
ReactantButyllithiumHCID 178418339—
Product4-(1,1-Dimethyl-4,4,4-trifluoro-2-butynyl)anisoleHCID 1867759013%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of Compound 56 (0.22 g, 1.26 mmol) in THF (8 ml) was added n-BuLi (1.69 M in hexane, 0.82 ml, 1.39 mmol) at −78° C. under N2, then warmed up to 0° C., and stirred for 1 h. S-(Trifluoromethyl)dibenzothiophenium trifluoromethane-sulfonate (1.01 g, 2.52 mmol) was added, and stirred for 3 h at 0° C. The mixture was quenched by the addition of NaHCO3 aq., and extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated. This was purified by SiO2 chromatography to give Compound 57 (38 mg, 13%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329396B1
Source datasetuspto-grants-2001_12
ORD IDord-65b09b873966426fb341b59ac38de3fc
Source noteuspto-grants-2001_12