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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253531생성일: 2026년 10월 25일

Hexane → (R)-tert-butyl 3-(3-chloro-2-fluorobenzoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/253531

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물1-Chloro-2-fluorobenzeneHCID 9583—
반응물(R)-tert-butyl 3-(N-methoxy-N-methylcarbamoyl)piperidine-1-carboxylateHCID 30025965—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(R)-tert-butyl 3-(3-chloro-2-fluorobenzoyl)piperidine-1-carboxylateHCID 5938284770.2%

반응 조건

온도-75 °C

반응 단계

To a stirred solution of 1-chloro-2-fluoro-benzene (13.0 g, 0.1 mol) in THF (250 mL) at −75° C. was added dropwise 2.5 M BuLi in hexane (40 mL, 0.1 mol) over 45 min. After additional stirring for 30 min at −75° C., a solution of (R)-tert-butyl 3-(methoxy(methyl)carbamoyl)-piperidine-1-carboxylate (21.76 g, 0.08 mol) in THF (100 mL) was added dropwise over 30 min. The mixture was allowed to warm from −70° C. to 0° C. The mixture was quenched with satd aq NH4Cl, extracted with EtOAc (3×) and the combined organic layers were dried over Na2SO4. Solvent removal and flash column chromatography, eluting with 5% EtOAc/PE afforded (R)-tert-butyl 3-(3-chloro-2-fluorobenzoyl)piperidine-1-carboxylate (19.2 g, 70%). 1H NMR (400 MHz, CDCl3): 1.45 (s, 9H), 1.63 (m, 2H), 1.76 (m, 1H), 2.06 (m, 1H), 2.87 (m, 1H), 3.15 (m, 1H), 3.25 (m, 1H), 3.9 (m, 1H), 4.2 (m, 1H), 7.18 (m, 1H), 7.60 (m, 2H). MS (E/Z): 342 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872028B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-2081c657440a426ebf725840f6df1689
출처 메모uspto-grants-2011_01