반응 #77644

ord-c7c05af2aecd4fb98518f03bcdbd2511

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 2 hours
  2. 2
    온도the medium is cooled
  3. 3
    여과After filtration
  4. 4
    기타the residue is purified by chromatography on silica gel (eluent: 95 heptane/5 ethyl acetate)

실험 절차

1 g (1.3 mmol) of (E)-6-{5-[3,4-bis(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]-2-thienyl}-1,1,1,-trifluoro-2-trifluoromethyloct-5-en-3-yn-2-ol is dissolved in 10 mL of THF and then added to a suspension of 160 mg (4.2 mmol) of lithium aluminium hydride and 450 mg (8.4 mmol) of sodium methoxide in 20 mL of THF. After stirring at reflux for 2 hours, the medium is cooled and then treated with 200 μL of water, 200 μL of 15% sodium hydroxide and 600 μL of water. After filtration, the residue is purified by chromatography on silica gel (eluent: 95 heptane/5 ethyl acetate). The desired product is obtained in the form of a yellow oil (210 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06706725B1uspto-grants-2004_03