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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774Generated: October 26, 2026

2-Aminobenzophenone → 2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenone

https://huagongshe.com/reaction/1774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzophenoneHCID 76080—
ReactantSodium BicarbonateHCID 516892—
SolventEthyl AcetateHCID 8857—
Product2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenoneHCID 53932370—

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-947d3e4afae94a0b8dd4f97535b58d90
Source noteuspto-grants-1998_03