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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953873Generated: November 2, 2026

Ethanethiol → 2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthalene

https://huagongshe.com/reaction/1953873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantTriethylamineHCID 8471—
Reactant7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthaleneHCID 22571521—

Reaction Steps

To a solution of 1.03 g (4.1 mmol) of 7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound G) in 30.0 mL of tetrahydrofuran, was added dropwise 0.49 g (0.85 ml, 7.8 mmol) of titaniumtetrachloride and the resulting solution stirred for 10 min. A solution of 35 mg (0.50 mL, 6.7 mmol) of ethanethiol and 0.54 g (0.75 mL, 5.4 mmol) of triethylamine in 10.0 mle of tetrahydrofuran was added and the reaction stirred at room temperature for 13 h. The mixture was diluted with water and extracted with ether (2x). The organic phase was washed with brine, dried over Na2SO4 and then concentrated in vacuo. Purification by flash chromatography (silica, 100% hexane) gave the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117987
Source datasetuspto-grants-2000_09
ORD IDord-faa8d1a968024b06aca0dc785a29824b
Source noteuspto-grants-2000_09