反応式
[F:1][CH2:2][C:3]1([CH2:19][F:20])[CH:8]=[C:7]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:6]2[CH:14]=[C:15](I)[CH:16]=[CH:17][C:5]=2[O:4]1.[F:21][C:22]([F:27])([F:26])C([O-])=O.[K+].C1(C)C=CC=CC=1>CN(C)C=O>[F:1][CH2:2][C:3]1([CH2:19][F:20])[CH:8]=[C:7]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:6]2[CH:14]=[C:15]([C:22]([F:27])([F:26])[F:21])[CH:16]=[CH:17][C:5]=2[O:4]1参加物
反応条件
- 温度
- 150 °C
実験手順
A mixture of 1.00 g of ethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylate, 0.84 g of potassium trifluoroacetate, 1.18 g of cuprous iodide, 4 ml of toluene and 10 ml of N,N-dimethylformamide was heated with stirring at 150° C. for 5.5 hours in a nitrogen gas atmosphere while removing toluene. The reaction mixture was added to a mixed solution of 2N hydrochloric acid and ethyl acetate, and an insoluble material was separated by filtration using celite. The organic layer was separated from the filtrate, and the aqueous layer was extracted with ethyl acetate. The resulting organic layers were combined, washed with a brine, dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography (an eluting solvent, ethyl acetate:hexane =10:1) to obtain 0.51 g of ethyl 2,2-bisfluoromethyl-6-trifluoromethyl-2H-1-benzopyran-4-carboxylate as an oily substance.
後処理
- temperaturewas heated
- customwhile removing toluene
- additionThe reaction mixture was added to a mixed solution of 2N hydrochloric acid and ethyl acetate
- customan insoluble material was separated by filtration
- customThe organic layer was separated from the filtrate
- extractionthe aqueous layer was extracted with ethyl acetate
- washwashed with a brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-2e1e4b4c1fbe43408df122cb91c8598a
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05646310
関連ノート
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