반응 #64847

ord-4a411b1b7007494db70c36a9bc8ed7aa

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with chloroform
  2. 2
    세척The chloroform phase was washed with a saturated saline solution
  3. 3
    기타dried on sodium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was distilled out under reduced pressure
  5. 5
    기타Residue was purified by silica gel column chromatography (Wako Gel C-200, 50 g)
  6. 6
    세척eluted with a mixed solvent of n-hexane (70 parts)+ethyl acetate (30 parts)

실험 절차

The above-mentioned 4-acryloyl-2-chloro-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (2.3 g) and anisole (1.1 g) were dissolved in methylene chloride (50 ml) and stannic chloride (2.8 g) was added thereto and agitated at room temperature for 2 hours. To the reaction mixture water was added and extracted with chloroform. The chloroform phase was washed with a saturated saline solution and dried on sodium sulfate and thereafter the solvent was distilled out under reduced pressure. Residue was purified by silica gel column chromatography (Wako Gel C-200, 50 g) and eluted with a mixed solvent of n-hexane (70 parts)+ethyl acetate (30 parts) to give 4-acryloyl-2-[4-methoxyphenyl]-7-methoxy-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.7 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05416066uspto-grants-1995_05