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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259190Generated: October 30, 2026

Hydrochloric Acid → 5-(1,3-Dithiolan-2-yl)resorcinol

https://huagongshe.com/reaction/259190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-EthanedithiolHCID 10902—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzaldehyde, 3,5-bis(acetyloxy)-HCID 14235923—
SolventDiethyl EtherHCID 3283—
Product5-(1,3-Dithiolan-2-yl)resorcinolHCID 1168715184%

Reaction Steps

Dry hydrogen chloride was bubbled into a solution of 50.0 g (0.23 mole) of 3,5-diacetoxybenzaldehyde and 21.4 g (0.23 mole) of 1,2-ethanedithiol in 25 ml of ether until the solution became warm. After allowing the solution to stand at ambient temperature for 0.75 hour, the solvent was removed in vacuo and excess methanol was added. A solid of 1,3-diacetoxy-5-(1,3-dithiolan-2-yl)benzene (mp 94°-96° C.) was separated by filtration. It was resuspended in 100 ml of methanol and 21.7 g (0.23 mole) of potassium hydroxide pellets were added. On stirring the mixture at ambient temperature for 0.5 hour, the mixture became homogeneous. The solvent was removed in vacuo and the residue after acidification with 6N hydrochloric acid was extracted with ethyll acetate. The extract was washed with water until neutral, dried and evaporated in vacuo to leave 5-(1,3-dithiolan-2-yl)resorcinol as a gum (41.3 g, 84%) which was used without further purification in the subsequent reaction. The structure was confirmed by the infrared and nuclear magnetic resonance spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036857
Source datasetuspto-grants-1977_07
ORD IDord-84fafa63ec0f42dda6e7772b8d0605a0
Source noteuspto-grants-1977_07