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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373545Generated: October 28, 2026

Sodium hydride → 3,4-dihydro-3,3-dimethyl-2H-1,5-benzodithiepine

https://huagongshe.com/reaction/373545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1,2-BenzenedithiolHCID 69370—
Reactant2,2-Dimethylpropanediol ditosylateHCID 21651464—
SolventDimethyl SulfoxideHCID 679—
Product3,4-dihydro-3,3-dimethyl-2H-1,5-benzodithiepineHCID 1993550963.1%

Reaction Steps

15 g of dimercaptobenzene were slowly added dropwise while cooling to 5.55 g of sodium hydride (50% in mineral oil) in 150 ml of dimethyl sulfoxide, whereby the internal temperature was held between 15° and 23° C. Subsequently, the reaction mixture was stirred at room temperature for 1 hour and cooled with ice/methanol. Thereafter, 50 g of 2,2-dimethylpropanediol ditosylate in solid form were added in one portion and the reaction mixture was heated to 80° C. for 3 hours. Thereafter, the reaction mixture was cooled, poured on to ice, extracted with ether, the extract was washed with water and dried. After evaporation of the solvent, there was obtained a yellow oil which was chromatographed on silica gel (petroleum ether/ethyl acetate 99:1). There were obtained 14 g of 3,4-dihydro-3,3-dimethyl-2H-1,5-benzodithiepine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164387
Source datasetuspto-grants-1992_11
ORD IDord-bee86677d3cf4bfaad6c842329a5d0a4
Source noteuspto-grants-1992_11