Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416136Generated: October 26, 2026

Triphenylphosphine → 4-(4-Bromo-3,5-dimethylphenoxy)thiane

https://huagongshe.com/reaction/416136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTetrahydro-2H-thiopyran-4-olHCID 576296—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromo-3,5-dimethylphenoxy)thianeHCID 5934255386.6%

Reaction Steps

To a solution of 4-bromo-3,5-dimethylphenol (0.201 g, 1.00 mmol), tetrahydro-2H-thiopyran-4-ol (0.130 g, 1.10 mmol) and triphenylphosphine (0.341 g, 1.30 mmol) in tetrahydrofuran (5 mL) was added diethyl azodicarboxylate (40% solution in toluene, 0.591 mL, 1.30 mmol), and the mixture was stirred at room temperature for 1.5 hr. Tetrahydro-2H-thiopyran-4-ol (0.0591 g, 0.500 mmol), triphenylphosphine (0.157 g, 0.600 mmol) and diethyl azodicarboxylate (40% solution in toluene, 0.272 mL, 0.600 mmol) were added, and the mixture was further stirred for 1.5 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=0:100-20:80) to give the title compound (0.261 g, yield 86%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088821B2
Source datasetuspto-grants-2012_01
ORD IDord-3134f61bedd645d5bd7952aaa17d57a5
Source noteuspto-grants-2012_01