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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881344Generated: October 26, 2026

Iodine → 1,2-Dithiolane

https://huagongshe.com/reaction/1881344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantDimercaptoacetyl monobenzalpentaerythritolHCID 131730077—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product1,2-DithiolaneHCID 79045—
Product2,2-Bis(hydroxymethyl)-4-phenylbut-3-ene-1,3-diolHCID 53445166—

Reaction Steps

A solution of dimercaptoacetyl monobenzalpentaerythritol (4.1 mmol) in EtOH (20 ml) is treated with 10 ml of aqueous 1 N NaOH at room temperature for 1 h. The mixture is diluted with CH2Cl2 (100 ml) and then an aqueous solution of 0.1 M iodine (4.5 mmol) is added dropwise. The reaction mixture was stirred for 2 hours at room temperature and 1 mmol of Na2S2O3 (1 M aqueous solution) was added to the reaction mixture. The organic phase was separated, washed with water (3(200 mL), dried with magnesium sulfate, and evaporated at room temperature. The crude product is chromatographed on silica gel (200 mL) using a solvent mixture of hexane and ethyl acetate (40:20) as eluent to give 1,2-dithiolane of monobenzalpentaerythritol. Step 5: Synthesis of 1,2-dithiolane pentaerythritol

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318795B2
Source datasetuspto-grants-2012_11
ORD IDord-94a34d52e5394d52a26b7a6e2cf10203
Source noteuspto-grants-2012_11