Methyl formate → HCID 86666219、化合物
反応式
[H-].[Na+].[F:3][C:4]([F:12])([F:11])[CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8].[CH:13](OC)=[O:14]>COCCOC>[F:3][C:4]([F:12])([F:11])[CH2:5]/[C:6](=[CH:13]/[OH:14])/[C:7]([O:9][CH3:10])=[O:8]参加物
5
実験手順
To a suspension of NaH (0.512 g, 12.81 mmol) in DME (15 mL) was added a solution of methyl 4,4,4-trifluorobutanoate (1 g, 6.41 mmol) and methyl formate (0.594 mL, 9.61 mmol) in DME (10 mL) dropwise at 0° C. The mixture was stirred at room temperature overnight. After removing the solvent, the residue was diluted with water (50 mL), extracted with ether once, and neutralized to pH<7 by AcOH. The aqueous layer was separated and extracted with EA twice. The combined organic phase was dried over sodium sulfate, filtered, and concentrated to afford the title compound (0.875 g, 4.75 mmol, 74.2% yield). LCMS: rt=2.23 min, [M+H+]=185
後処理
- customAfter removing the solvent
- additionthe residue was diluted with water (50 mL)
- extractionextracted with ether once
- customThe aqueous layer was separated
- extractionextracted with EA twice
- dry with materialThe combined organic phase was dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-5dc5507b6fc44d6aace00df2603b5236
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637536B2
反応ノート
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