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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986247Generated: October 30, 2026

Potassium Carbonate → (2-Chlorophenyl)(2,2-diethoxyethyl)sulfane

https://huagongshe.com/reaction/1986247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactanto-ChlorothiophenolHCID 80599—
SolventAcetoneHCID 180—
Product(2-Chlorophenyl)(2,2-diethoxyethyl)sulfaneHCID 59133109—

Reaction Steps

Into a 2 L round bottomed flask is added 2-chlorobenzenethiol (50.0 g, 346 mmol), potassium carbonate (52.7 g, 381 mmol) and acetone (1 L). 2-Bromo-1,1-diethoxyethane (71.5 g, 363 mmol) is added and the mixture is heated to reflux for 24 hours. The cooled mixture is filtered and concentrated under reduced pressure to yield crude 2-chlorophenyl-(2,2-diethoxyethyl)sulfane as a pale pink oil (101.8 g, quantitative). A 2 L, 3-necked round-bottomed flask, fitted with a mechanical stirrer, condenser and addition funnel is charged with chlorobenzene (1 L) and polyphosphoric acid (200 g) and the mixture is heated to reflux. At reflux the crude (2-chlorophenyl)(2,2-diethoxyethyl)sulfane is added dropwise over 1.5 hours and the mixture is refluxed for a further 24 hours. The cooled organic layer is decanted and concentrated under reduced pressure. The crude material is subjected to chromatography on silica (hexane) to provide the title compound as a brown oil (54.4 g, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-4f219712091d42eba7f1ebf535e5becb
Source noteuspto-grants-2009_06