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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773Generated: October 26, 2026

Thionyl Chloride → 5-Oxotetrahydro-2-furancarbonyl chloride

https://huagongshe.com/reaction/1773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-Oxo-2-tetrahydrofurancarboxylic acidHCID 251524—
Product5-Oxotetrahydro-2-furancarbonyl chlorideHCID 10844540—

Reaction Steps

A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726306
Source datasetuspto-grants-1998_03
ORD IDord-c2d7b50a1bd84d1e8cef8cf871d36f05
Source noteuspto-grants-1998_03