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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481228Generated: October 25, 2026

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

https://huagongshe.com/reaction/481228

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 pruduct 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 numberUS06653483B1
Source datasetuspto-grants-2003_11
ORD IDord-34bd848d7906436a8855b2305c9e81c6
Source noteuspto-grants-2003_11