反応式
[F:1][C:2]([Si](C)(C)C)([F:4])[F:3].[Br:9][C:10]1[CH:15]=[CH:14][C:13]([CH:16]([CH3:30])[C:17]([C:19]2[CH:29]=[CH:28][C:22]3[N:23]([CH3:27])[C:24](=[O:26])[O:25][C:21]=3[CH:20]=2)=[O:18])=[C:12]([Cl:31])[CH:11]=1.O.O.O.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[Br:9][C:10]1[CH:15]=[CH:14][C:13]([CH:16]([CH3:30])[C:17]([C:19]2[CH:29]=[CH:28][C:22]3[N:23]([CH3:27])[C:24](=[O:26])[O:25][C:21]=3[CH:20]=2)([OH:18])[C:2]([F:4])([F:3])[F:1])=[C:12]([Cl:31])[CH:11]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
Trifluoromethyltrimethylsilane (2M in THF, 1.48 mL) was added at 0° C. to a solution of 6-[2-(4-bromo-2-chloro-phenyl)-propionyl]-3-methyl-3H-benzooxazol-2-one (531 mg) in THF (15 mL) followed by the addition of tetrabutylammonium fluoride trihydrate (424 mg). Stirring was continued for 48 hours at r.t. The reaction mixture was poured into ice/water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, heptane:ethyl acetate=7:3) to give the title compound as a orange amorphous foam (440 mg, 70%). MS (neg. ion, m/e)=464.0 [(M−H)−].
後処理
- extractionextracted two times with ethyl acetate
- washThe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- customthe solvent was evaporated
- customThe residue was purified by flash chromatography (silica gel, heptane:ethyl acetate=7:3)
出典と根拠
- ORDレコード
- ord-e50e34910bc647dca7dbd92d3f0f4d69
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08268820B2
関連ノート
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