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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379640Generated: October 25, 2026

1-(Chloromethyl)-4-(methylthio)benzene → 2-Methyl-3-(4-methylthiobenzyl)-1-indanone

https://huagongshe.com/reaction/379640

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethyl)-4-(methylthio)benzeneHCID 70128—
Reactant2-MethylindanoneHCID 249262—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-3-(4-methylthiobenzyl)-1-indanoneHCID 18367456—

Reaction Steps

To a cooled solution (−70° C.) of LDA (1 M) in THF (37 mL) was added dropwise a solution of 2-methyl-1-indanone (J.A.C.S. Vol. 98, 8119-8124 (1976)) (2.5 g, 17 mmol) in THF (20 mL). The resulting dark red solution was stirred at room temperature for 3 hours, then cooled to −20° C. and a solution for 4-methylthiobenzyl chloride (3.1 g, 18 mmol) in THF (15 mL) was added slowly. The addition completed, the reaction mixture was stirred at −20° C. for 30 minutes before being quenched with 3N aqueous HCl (50 mL) and brine (50 mL). The product was extracted with ether, dried over MgSO4 and evaporated to dryness. The oily residue was chromatographed on silica gel eluting with a 1:5 mixture of ethyl acetate-hexane to afford the pure title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300346B1
Source datasetuspto-grants-2001_10
ORD IDord-6e463c8082fe4fbbbdd06b9eff4ef69d
Source noteuspto-grants-2001_10