تفاعل #1330390

ord-681f15629df742b88e6fee5ad0b13ded

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe reaction mixture was then filtered
  2. 2
    تركيزconcentrated to a small volume
  3. 3
    أخرىpurified by silica gel column chromatography with a 0–25% ethyl acetate in hexanes gradient

الإجراء التجريبي

A solution of (+)-(1S,4R)-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enol (1.43 g, 6.67 mmol) (from Example 29a supra) and Wilkinson's catalyst (1.23 g, 1.33 mmol) (Aldrich) in toluene (55 mL) was subjected to atmospheric pressure hydrogenation for 16.5 hours. The reaction mixture was then filtered, concentrated to a small volume, and purified by silica gel column chromatography with a 0–25% ethyl acetate in hexanes gradient to give (+)-(1R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-cyclopentanol as a colorless oil. (Yield 745 mg, 61%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07115740B2uspto-grants-2006_10