HRID1764721

反应详情

EQUATION

反应方程式

HRID 1764721 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A mixture of 50 g of 3-nitro-8,9-dihydro [5H] benzocycloheptene-5-one, 1200 ml of methanol, 120 ml of tetrahydrofuran, 100 ml of a 10% aqueous potassium carbonate and 50 ml of acetone cyanhydrin under nitrogen was refluxed for an hour in a bath at 90° C. and the mixture was concentrated to about 200 ml under reduced pressure. The mixture was cooled to 20° C. and was extracted with methylene chloride. The organic phase was washed with water, dried and distilled to dryness under reduced pressure. The 58 g of brown oil residue were crystallized from 50 ml of methanol and the mixture was vacuum filtered to obtain 46 g of 3-nitro-5-oxo-6,7,8,9-tetrahydro [5H] benzocycloheptene-7-carbonitrile with a melting point of 107° C. and then 120° C.

WORKUP

后处理

  1. concentrationthe mixture was concentrated to about 200 ml under reduced pressure
  2. temperatureThe mixture was cooled to 20° C.
  3. extractionwas extracted with methylene chloride
  4. washThe organic phase was washed with water
  5. customdried
  6. distillationdistilled to dryness under reduced pressure
  7. customThe 58 g of brown oil residue were crystallized from 50 ml of methanol
  8. filtrationfiltered