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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419031Generated: October 31, 2026

Thionyl Chloride → 5-Oxotetrahydro-2-furancarbonyl chloride

https://huagongshe.com/reaction/1419031

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 numberUS05885979
Source datasetuspto-grants-1999_03
ORD IDord-c8132c9b08414716aa0545424e03200d
Source noteuspto-grants-1999_03