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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394184Generated: November 1, 2026

Thiophenol → 4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene

https://huagongshe.com/reaction/2394184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
Product4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthaleneHCID 15896018—

Reaction Steps

To a stirred solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G, 1.48 g, 5.9 mmol), titanium tetrachloride (1.09 g, 5.7 mmol) and THF (10 mL) was added a mixture of thiophenol (660 mg, 6 mmol), triethylamine (1.16 g, 11.5 mmol) and THF (20 mL) via an addition funnel at ambient temperature. The mixture was stirred for 5 h, and water (10 mL) was added, extracted with ether (3×50 mL). The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4) and the solvent distilled off at reduced pressure. After silica gel chromatography the title compound was obtained as a colorless oil .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05808124
Source datasetuspto-grants-1998_09
ORD IDord-612895c5399b40a8b87fb6ec425f3bd5
Source noteuspto-grants-1998_09