반응 #413371

반응 방정식

(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

용매

acetonitrile

ether

hexane

반응 조건

후처리

1. 1
   여과filtered
2. 2
   기타The residue from the evaporation
3. 3
   추출was extracted with a mixture of 5 ml of ether and 95 ml of hexane
4. 4
   여과filtered
5. 5
   농축concentrated to dryness under vacuum
6. 6
   기타The residue was purified by column chromatography on silica gel with hexane/20-50% ethyl acetate as the eluent

실험 절차

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.

출처