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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15729생성일: 2026년 10월 23일

Ammonium Hydroxide → Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/15729

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물Ammonium ChlorideHCID 25517—
반응물Benzyl 3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylateHCID 11368235—
반응물HCID 178478191HCID 178478191—
반응물HCID 178494437HCID 178494437—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylateHCID 59342393—

반응 조건

온도-78 °C

반응 단계

CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732609B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ab71bfae619241b3a6352d150f024773
출처 메모uspto-grants-2010_06