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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539690생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/539690

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,2-DibromoethaneHCID 7839—
반응물4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물MagnesiumHCID 5462224—
반응물Potassium sodium tartarateHCID 9855836—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylateHCID 8668086259.6%

반응 조건

온도-78 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871766B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-313a2d8d585047c8b67d6c06f4797822
출처 메모uspto-grants-2014_10