Methanol → HCID 69557998、化合物

HRID 278278ノート

反応式

HRID 278278 の反応式
[OH:1][CH2:2][C@@H:3]1[CH2:7][C:6](=C)[CH2:5][C@H:4]1[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[CH:10]=1.C[OH:17]>>[OH:1][CH2:2][C@H:3]1[C@H:4]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([F:15])[CH:10]=2)[CH2:5][C:6](=[O:17])[CH2:7]1

参加物

3

実験手順

A solution of (+)-trans-1-hydroxymethyl-4-methylene-2-(3-fluorophenyl)cyclopentane from Step C (1.87 g, 9.0 mmol) in methanol (75 mL) was cooled in a dry ice/acetone bath and ozone was bubbled into the solution until the blue color persisted. The excess ozone was removed with a stream of nitrogen and then dimethylsulfide (5 mL) was added. After 10 min, the bath was removed and the reaction was allowed to warm to rt over 2 h. The mixture was treated with 10 drops of sulfuric acid (c) in water (2 mL) for 1 h before most of the methanol was removed in vacuo. The mixture was diluted with water and extracted twice with ethyl acetate and the organic layers were washed with brine, dried over sodium sulfate, combined and concentrated. The residue was purified by FC (50% ethyl acetate in hexanes) to give the title compound (1.87 g)), [α]D=+132 (MeOH, c=1.2).

後処理

  1. customozone was bubbled into the solution until the blue color
  2. customThe excess ozone was removed with a stream of nitrogen
  3. additiondimethylsulfide (5 mL) was added
  4. customthe bath was removed
  5. additionThe mixture was treated with 10 drops of sulfuric acid (c) in water (2 mL) for 1 h before most of the methanol
  6. customwas removed in vacuo
  7. additionThe mixture was diluted with water
  8. extractionextracted twice with ethyl acetate
  9. washthe organic layers were washed with brine
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated
  12. customThe residue was purified by FC (50% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-8f82f830395e4404b5edaa16bf0ae9fe
出典データセット
uspto-grants-2002_03
特許番号
US06358979B1

反応ノート

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