反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:14][S:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[F:22])[C:9]([O:11]CC)=[O:10])=[CH:4][CH:3]=1.C(O)=O.CS(O)(=O)=O.O>C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:14][S:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[F:22])[C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1参加物
6
実験手順
The crude ester from Step B (5.3 g, 16 mmole) was combined with 20 ml of 88% formic acid and 2.1 ml (33 mmole) of methane sulfonic acid. The emulsion was refluxed for five hours during which time it gradually became homogeneous. After cooling, water and methylene chloride were added and the aqueous phase was separated and extracted twice with methylene chloride. The organic phases were combined, dried (MgSO4) and concentrated. The crude residue was taken up in 4% ethyl acetate/hexane and filtered through a plug of silica gel to remove nonpolar impurities. The product acid was then rinsed from the silica gel with ethyl acetate and the solvent concentrated. The acid was a colorless solid (4.5 g, 95% yield).
後処理
- temperatureThe emulsion was refluxed for five hours during which time it gradually became homogeneous
- temperatureAfter cooling
- customthe aqueous phase was separated
- extractionextracted twice with methylene chloride
- dry with materialdried (MgSO4)
- concentrationconcentrated
- filtrationfiltered through a plug of silica gel
- customto remove nonpolar impurities
- washThe product acid was then rinsed from the silica gel with ethyl acetate
- concentrationthe solvent concentrated
出典と根拠
- ORDレコード
- ord-8cdbd7dd22044086b154fbbbd24fafa7
- 出典データセット
- uspto-grants-1993_01
- 特許番号
- US05182303
関連ノート
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