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HRID 29754作成日:2026年10月24日

Hydrochloric Acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/29754

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
反応物DiboronHCID 6328200—
反応物HCID 178418361HCID 178418361—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081100.2%

反応手順

To a solution of piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (19.3 g, 84.0 mmol) in THF (100 mL) was added diborane (185 mL, 1.0 M solution in THF) over a period of 10 min at 0° C. Hydrogen gas was rapidly evolved and after gas evolution had ceased the reaction was stirred at room temperature for 1 h. The reaction mixture was again cooled to 0° C., and 1 M aqueous HCl was added dropwise to the reaction mixture with further evolution of hydrogen. Addition of HCl was continued until the evolution of hydrogen had almost ceased. The mixture was then stirred for 10 min and made basic (pH 13-14) by the addition of 1 M NaOH solution. The aqueous solution was extracted with ethyl acetate, the organic phase washed with brine, dried and concentrated under reduced pressure to yield 4-Hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester (18.12 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423012B2
出典データセットuspto-grants-2008_09
ORD IDord-91d40b688a9b498cabf1e210a690dcf9
出典メモuspto-grants-2008_09