تفاعل #1870

ord-947d3e4afae94a0b8dd4f97535b58d90

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726306uspto-grants-1998_03