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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925257Generated: October 30, 2026

1,2-Ethanedithiol → HCID 86645389, compound

https://huagongshe.com/reaction/925257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-EthanedithiolHCID 10902—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67521261HCID 67521261—
SolventDichloromethaneHCID 6344—
ProductHCID 86645389HCID 8664538966.1%

Reaction Steps

To a solution of acetic acid [3-(4-fluorophenyl)-3-oxo-propyl]ester (2.0 g, 9.52 mmol) in dry dichloromethane (40 ml) are added 1,2-ethanedithiol (1.79 g, 19.0 mmol) and boron trifluoride diethyl ether complex (0.68 g, 4.76 mmol) at 0° C. The resulting reaction mixture is stirred at RT for 16 h. After completion of reaction, the mixture is neutralized with 10M aqueous sodium hydroxide and extracted with DCM (3×100 ml). The combined organic layers are washed with water (100 ml), brine (100 ml), dried over anhydrous sodium sulfate and evaporated in vacuo to get the crude, which is purified by column chromatography (silica gel, 5% ethyl acetate/hexane) to yield acetic acid 2-[2-(4-fluorophenyl)-[1,3]dithiolan-2-yl]-ethyl ester (1.80 g, 6.29 mmol, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284286B2
Source datasetuspto-grants-2016_03
ORD IDord-ae9cee90a3d849b8b38d649f0af75e2b
Source noteuspto-grants-2016_03