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HRID 60603作成日:2026年10月25日

Hydrochloric Acid → Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/60603

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1,2-DibromoethaneHCID 7839—
反応物4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物MagnesiumHCID 5462224—
反応物Potassium sodium tartarateHCID 9855836—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 8668086259.6%

反応条件

温度-78 °C

反応手順

To a suspension of magnesium (1.2 g) and 1,2-dibromoethane (0.11 mL) in diethyl ether (30 mL) was added a solution of 3,4-difluorobenzyl bromide (10 g) in diethyl ether (10 mL) at room temperature under a nitrogen atmosphere, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with THF (30 mL), and cooled to −78° C. A solution of tert-butyl 4-oxopiperidine-1-carboxylate (5.0 g) in THF (10 mL) was added thereto, and the mixture was allowed to warm to room temperature, and was stirred overnight. To the reaction mixture was added a small amount of 1N hydrochloric acid at 0° C. to quench the reaction. Saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane), and recrystallized from ethyl acetate/hexane to give the title compound (4.9 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440990B2
出典データセットuspto-grants-2016_09
ORD IDord-214c48bfee4249b7bec1a5a8f75a7ad3
出典メモuspto-grants-2016_09