Triacetoxyperiodinane → 1-(3,5-Dimethylphenyl)-5-(5-fluoro-2-methoxyphenyl)-3-methoxymethoxy-5-methyl-3-trifluoromethylhexan-2-one

HRID 916015ノート

反応式

HRID 916015 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH2:9][CH:10]([OH:33])[C:11]([O:29][CH2:30][O:31][CH3:32])([C:25]([F:28])([F:27])[F:26])[CH2:12][C:13]([C:16]2[CH:21]=[C:20]([F:22])[CH:19]=[CH:18][C:17]=2[O:23][CH3:24])([CH3:15])[CH3:14])[CH:5]=[C:6]([CH3:8])[CH:7]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C1=CC=CC=2)=O>ClCCl>[CH3:8][C:6]1[CH:5]=[C:4]([CH2:9][C:10](=[O:33])[C:11]([O:29][CH2:30][O:31][CH3:32])([C:25]([F:26])([F:27])[F:28])[CH2:12][C:13]([C:16]2[CH:21]=[C:20]([F:22])[CH:19]=[CH:18][C:17]=2[O:23][CH3:24])([CH3:15])[CH3:14])[CH:3]=[C:2]([CH3:1])[CH:7]=1

参加物

4

実験手順

To a solution of 137 mg (0.29 mmol) of 1-(3,5-dimethylphenyl)-5-(5-fluoro-2-methoxyphenyl)-3-methoxymethoxy-5-methyl-3-trifluoromethylhexan-2-ol (Example 12) in dichloromethane was added 350 mg (0.82 mmol) of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3-(1H)-one (Dess-Martin periodinane). After 1 hour, the reaction was quenched with saturated sodium bicarbonate, and filtered through diatomaceous earth, washing with EtOAc. The organic layer was separated and the basic aqueous phase extracted with two 5 mL portions of EtOAc. The combined organic layers were washed with 5 mL of saturated aqueous sodium bicarbonate, three 5 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude material was purified on a prep plate (2 mm, silica gel, EtOAc-hexanes (1:9), 3×developed) to afford 84 mg (61%) of 1-(3,5-dimethylphenyl)-5-(5-fluoro-2-methoxyphenyl)-3-methoxymethoxy-5-methyl-3-trifluoromethylhexan-2-one.

後処理

  1. customthe reaction was quenched with saturated sodium bicarbonate
  2. filtrationfiltered through diatomaceous earth
  3. washwashing with EtOAc
  4. customThe organic layer was separated
  5. extractionthe basic aqueous phase extracted with two 5 mL portions of EtOAc
  6. washThe combined organic layers were washed with 5 mL of saturated aqueous sodium bicarbonate, three 5 mL portions of brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe crude material was purified on a prep plate (2 mm, silica gel, EtOAc-hexanes (1:9), 3×developed)

出典と根拠

ORDレコード
ord-b99686befcd84b5591b973a90cbcdc33
出典データセット
uspto-grants-2007_09
特許番号
US07268152B2

反応ノート

読み込み中…