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HRID 501314作成日:2026年10月26日

Potassium tert-butoxide → 4-(5-Trifluoromethyl-benzo[d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/501314

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-5-trifluoromethyl-phenyl)-hydroxyiminomethyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 72434547—
溶媒TetrahydrofuranHCID 8028—
生成物4-(5-Trifluoromethyl-benzo[d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 58817530106.1%

反応手順

A solution of 4-[(2-Fluoro-5-trifluoromethyl-phenyl)-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl ester (4.969 g, 0.013 M) in anhydrous THF (59 mL) was treated with Potassium tert-butoxide (13.4 mL of a 1M solution in THF, 0.0133 M-1.05 eq). The mixture was stirred at ambient temperature for 1 hour and then heated to 65° C. for 2 hours. The THF was removed under reduced pressure. The residue was dissolved in ethyl acetate (100 mL), washed with H2O (50 mL) and brine (50 mL) respectively. It was then dried over MgSO4, filtered and concentrated to give a solid (5 g) which was purified on silica ˜120 g, (eluting with ethylacetate heptane (30:70) to give the product as a white solid (2.69 g, 57%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772252B2
出典データセットuspto-grants-2010_08
ORD IDord-cc987dde104b489ab6857cf32d915e8a
出典メモuspto-grants-2010_08