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HRID 2407642作成日:2026年10月26日

Sulfuric Acid → 5H-Octafluoropentanoic acid

https://huagongshe.com/reaction/2407642

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物2,2,3,3,4,4,5,5-Octafluoro-1-pentanolHCID 9641—
反応物Potassium BromideHCID 253877—
反応物TempoHCID 2724126—
反応物Sodium HypochloriteHCID 23665760—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物5H-Octafluoropentanoic acidHCID 120227—

反応手順

5.2 ml water, 19 ml MeCN, 0.34 g KBr, TEMPO (0.12 g), and 6 g of 2,2,3,3,4,4,5,5-octafluoro-pentan-1-ol were placed in a 100 mL glass flask equipped with a dropping funnel and stirrer. 45 mL of 15% (wt) aq. NaOCl buffered to pH 8-9 were added via the dropping funnel in 3 portions over two days while stirring at room temperature. Then concentrated sulphuric acid were added to render the reaction mixture acidic. (pH 1-2). The reaction mixture was extracted three times with diethyl ether and the combined organic phases were dried over magnesium sulphate. The solvent was evaporated to give a colorless liquid (8.98 g), which was distilled using a water pump (15 mmHg, 73° C.) to give 5.13 g of the acid. Yield: 80%. 1H NMR (CDCl3): 6.08 (tt, J=52 Hz, J=5.3 Hz, 1H); 8.6 (s, 1H); 19F NMR (CDCl3): −120.6 (t, J=9.2 Hz, 2F); −125.81 (m, 2F); −130.61 (m, 2F); −138.4 (dm, J=52 Hz, 2F).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08809580B2
出典データセットuspto-grants-2014_08
ORD IDord-b55ef902930d446496332faeba9a26a4
出典メモuspto-grants-2014_08