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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691524Generated: October 26, 2026

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

https://huagongshe.com/reaction/1691524

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% toluene solution, 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% toluene solution, 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 numberUS08153694B2
Source datasetuspto-grants-2012_04
ORD IDord-ad9aeda83b994ecaa1562fcc622a8f8a
Source noteuspto-grants-2012_04