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HRID 603378作成日:2026年10月26日

Water → 7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-ol

https://huagongshe.com/reaction/603378

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oximeHCID 136340076—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-olHCID 13580081250%

反応条件

温度0 °C

反応手順

1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oxime (4.2 g, 15.96 mmol, prepared by the method described in WO9728137) and PPh3 (8.82 g, 33.6 mmol) were dissolved in THF (250 mL), and the mixture was cooled to 0° C. A solution of DEAD (5.02 mL, 32.0 mmol) in THF (150 mL) was slowly added over a period of 30 min. The reaction mixture was stirred for 1 h at 0° C. After addition of water (500 mL) and extraction with EtOAc (3×300 mL), the combined organic phases were washed with brine (300 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The product was purified by silica gel flash chromatography (1:6 EtOAc/hexane) to yield 1.96 g (50%) of the title compound as a light yellow powder. 1H NMR (300 MHz, CDCl3): δ 1.00 (t, 3H), 1.73 (m, 2H), 2.88 (t, 2H), 5.34 (s, 1H), 6.93 (d, 1H), 7.48 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906653B2
出典データセットuspto-grants-2011_03
ORD IDord-83ffd2f5ab7c4aedbb33add5f1d566ba
出典メモuspto-grants-2011_03