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HRID 501320作成日:2026年10月25日

Water → 4-[(2-Fluoro-3-trifluoromethylphenyl)-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/501320

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PyridineHCID 1049—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物4-(2-Fluoro-3-trifluoromethyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 58817540—
溶媒Ethylacetate heptaneHCID 21899848—
生成物4-[(2-Fluoro-3-trifluoromethylphenyl)-hydroxyimino-methyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 7243456791%

反応手順

A mixture of 4-(2-Fluoro-3-trifluoromethyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester (9.00 g, 24.0 mmol), hydroxylamine hydrochloride (2.00 g, 28.8 mmol) and pyridine (50 mL) was stirred at room temperature under nitrogen overnight. The yellow reaction solution was poured into cold water (500 mL) and the mixture aged at 0° C. for 1 h. The product was collected by filtration, washed with water, and dried under vacuum at 50° C. to afford 9.54 g of a while solid. Trituration of the solid with hot 25% ethyl acetate/heptane afforded 8.50 g (91%) of the desired product as a white solid. Proton NMR showed product to be a 3.8 to 1 mixture of isomers.

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-4fe4a48a5a504448a2d574a082643679
出典メモuspto-grants-2010_08