反応 #413375

ord-6e7ee041d3a44c44a652379d65b311b1

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過filtered
  2. 2
    抽出The evaporation residue was extracted with a mixture of 5 ml of ether and 95 ml of hexane
  3. 3
    ろ過filtered
  4. 4
    濃縮concentrated to dryness under vacuum
  5. 5
    その他The residue was purified by column chromatography on silica gel with hexane/10-50% ethyl acetate as the eluent

実験手順

A solution of 1.16 g of (5Z,13E,18Z)-(8R,9S,11R,12R,15S,16RS)-9-hydroxy-19-chloro-16-methyl-11,15-bis(tetrahydropyran-2-yloxy)-5,13,18-prostatrienoic acid methyl ester, 785 mg of triphenylphosphine, and 15 ml of a solution of 0.97 ml of carbon tetrachloride, 0.79 ml of pyridine, and 48 ml of acetonitrile was stirred under argon at room temperature for 65 hours. The mixture was then diluted with 15 ml of ether and 30 ml of hexane, further stirred for 10 minutes, and filtered. The evaporation residue was extracted with a mixture of 5 ml of ether and 95 ml of hexane, filtered, and concentrated to dryness under vacuum. The residue was purified by column chromatography on silica gel with hexane/10-50% ethyl acetate as the eluent. In this way, 457 mg of the desired compound was isolated.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04444788uspto-grants-1984_04