Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24572Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/24572

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 mL of tetrahydrofuran was added and the reaction stirred at room temperature for 13 h. The mixture was diluted with water and extracted with ether (2×). 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 numberUS06855832B2
Source datasetuspto-grants-2005_02
ORD IDord-57924e275c8e4ebe90a25748051ba105
Source noteuspto-grants-2005_02