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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220196Generated: October 29, 2026

Thionyl Chloride → HCID 22026129, compound

https://huagongshe.com/reaction/2220196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22026130HCID 22026130—
ProductHCID 22026129HCID 22026129—

Reaction Conditions

Temperature85 °C

Reaction Steps

4-(Ethoxycarbonyl)-5,6-dihydro-2H-pyran-3-sulfonic acid (27.5 g) was dissolved in thionyl chloride (82.6 ml) and the mixture was stirred at room temperature→85° C. for 3 h. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in ethyl acetate (100 ml). The obtained solution was partitioned by adding diluted brine (120 ml). The ethyl acetate layer was washed twice with saturated brine (50 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated and the obtained residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/7→1/5). The objective product was concentrated under reduced pressure and the crystals produced by freezing were washed with hexane to give ethyl 5-(chlorosulfonyl)-3,6-dihydro-2H-pyran-4-carboxylate (7.81 g) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417059B2
Source datasetuspto-grants-2008_08
ORD IDord-d9c5cd1e676e42a9b7e77cf9e1fd14c7
Source noteuspto-grants-2008_08