反応 #413371

反応方程式

(5Z,13E)-(8R,9S,11R,12R,15R)-9-hydroxy-11,15-bis(tetrahydropyran-2-yloxy)-16,16,19-trimethyl-5,13,18-prostatrienoic acid methyl ester

triphenylphosphine

carbon tetrachloride

pyridine

→

desired compound

(5Z,13E)-(8R,9R,11R,12R,15R)-9-Chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,16,19-trimethyl-5,13,18-prostatrienoic Acid Methyl Ester

溶媒

acetonitrile

ether

hexane

反応条件

後処理

1. 1
   ろ過filtered
2. 2
   その他The residue from the evaporation
3. 3
   抽出was extracted with a mixture of 5 ml of ether and 95 ml of hexane
4. 4
   ろ過filtered
5. 5
   濃縮concentrated to dryness under vacuum
6. 6
   その他The residue was purified by column chromatography on silica gel with hexane/20-50% ethyl acetate as the eluent

実験手順

A solution of 1.15 g of (5Z,13E)-(8R,9S,11R,12R,15R)-9-hydroxy-11,15-bis(tetrahydropyran-2-yloxy)-16,16,19-trimethyl-5,13,18-prostatrienoic acid methyl ester, 780 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 for 55 hours under argon at room temperature. The mixture was then diluted with 15 ml of ether and 30 ml of hexane, further stirred for 10 minutes, and filtered. The residue from the evaporation 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/20-50% ethyl acetate as the eluent, thus obtaining 1.07 g of the desired compound.

出典