Reaction #1869

ord-c2d7b50a1bd84d1e8cef8cf871d36f05

Reaction equation

O=C1CCC(C(=O)O)O1
5-oxotetrahydrofuran-2-carboxylic acid
O=S(Cl)Cl
thionyl chloride
O=C1CCC(C(=O)Cl)O1
5-oxotetrahydrofuran-2-carbonyl chloride

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperatureto reflux for 2 hours
  2. 2
    workup.DISTILLATIONThionyl chloride was then distilled off under reduced pressure

Procedure

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726306uspto-grants-1998_03