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HRID 456546作成日:2026年10月26日

Potassium tert-butoxide → 4-(7-Trifluoromethyl-benzo[d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/456546

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium tert-butoxideHCID 23665647—
反応物4-[(2-Fluoro-3-trifluoromethylphenyl)-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 72434567—
溶媒TetrahydrofuranHCID 8028—
生成物4-(7-Trifluoromethyl-benzo[d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 5881760273%

反応条件

温度60 °C

反応手順

To a room temperature mixture of 4-[(2-fluoro-3-trifluoromethyl-phenyl)-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl ester (1.40 g, 3.59 mmol) in THF (20 mL) under nitrogen was added potassium tert-butoxide (3.60 mL of a 1 M THF solution, 3.60 mmol) in one portion and the reaction heated at 60° C. for 1.5 h. After standing at room temperature overnight, the solvent was removed and the residue diluted with ethyl acetate (60 mL). The organics were washed with water (30 mL) and brine (30 mL) successively, dried over magnesium sulfate, filtered, and concentrated to give an amber solid. The crude product was chromatographed on silica using 40% ethyl acetateiheptane as eluent to afford 0.97 g (73%) of the desired product as a white solid, mp:111–113° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07186724B2
出典データセットuspto-grants-2007_03
ORD IDord-ffa0b744d9e3421c86c0c64eb40f7672
出典メモuspto-grants-2007_03