反应 #6334

ord-4f75d89850dd4de3a07f2755539ba444

反应方程式

CCOC(=O)CCc1cc(=O)oc2cc(OC)ccc12
3
CCOC(=O)CCc1cc(=O)oc2cc(OC)ccc12
4-(2-carbethoxy-1-ethyl)-7-methoxy-2-oxo-2H-1-Benzopyran
[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
CCS
EtSH
CCOC(=O)CCc1cc(=O)oc2cc(O)ccc12
4
收率 27.1%
CCOC(=O)CCc1cc(=O)oc2cc(O)ccc12
4-(2-carbethoxy-1-ethyl)-7-hydroxy-2-oxo-2H-1-Benzopyran
收率 27.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The ice bath was removed
  2. 2
    其他The solvents were removed in vacuo
  3. 3
    其他the residue thoroughly vacuum dried
  4. 4
    萃取The residue was extracted into EtOAc as much as possible, then the extract
  5. 5
    其他chromatographed

实验过程

To a suspension of 726 mg (5.4 mmol) of AlCl3 in 10 mL of dichloromethane at 0° C. was added 4 mL of EtSH. The suspension became a clear solution within seconds. Then, 298 mg (1.08 mmol) of 3 in 4 mL of dichloromethane was added, turning the yellow solution red in color. The ice bath was removed, and the reaction stirred to room temperature for 3 h. The solvents were removed in vacuo, and the residue thoroughly vacuum dried. The residue was extracted into EtOAc as much as possible, then the extract was flash chromatographed using 30/70 EtOAc/hexane. The long- and short-wave UV active band gave 76.7 mg (27%) of 4.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05247099uspto-grants-1993_09