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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396Generated: October 23, 2026

Water → Methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylate

https://huagongshe.com/en/reaction/1396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThiophenolHCID 7969—
ReactantTriethylamineHCID 8471—
ReactantMethyl 5,5-dimethyl-5,6 dihydro-naphthalen-8(7h)-one-2-carboxylateHCID 10681077—
CatalystTitanium TetrachlorideHCID 24193—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylateHCID 22571588—

Reaction Steps

To a solution of methyl-5,5-dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylate (Compound E2, 835.0 mg, 3.60 mmol) in 25.0 mL of THF at room temperature was added TiCl4 (670.0 mg, 3.55 mmol). Thereafter a solution of thiophenol (430.0 mg, 3.90 mmol) and Et3N (730.0 mg, 7.20 mmol) in 10 mL THF was added. The resulting brown mixture was stirred for 6 h before H2O was carefully added to quench the reaction. The product was extracted into Et2O and the combined organic layers washed with saturated aqueous NaCl and dried over MgSO4. Removal of the solvents under reduced pressure afforded a solid from which the title compound was isolated as a yellow solid by column chromatography (5% EtOAc-hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723666
Source datasetuspto-grants-1998_03
ORD IDord-83bf3c1c076c4485b404b1a77f65cfe6
Source noteuspto-grants-1998_03