Reaction #1870

ord-947d3e4afae94a0b8dd4f97535b58d90

Reaction equation

Nc1ccccc1C(=O)c1ccccc1
2-aminobenzophenone
O=C([O-])O.[Na+]
sodium hydrogencarbonate
O=C1CCC(C(=O)Nc2ccccc2C(=O)c2ccccc2)O1
2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    WashThe ethyl acetate layer was washed with water
  2. 2
    Dryingdried over anhydrous magnesium sulfate
  3. 3
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  4. 4
    OtherThe residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1)

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