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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132201생성일: 2026년 10월 24일

Toluene → Tert-butyl 4-(1-methoxy-3-(2-nitrophenyl)-1-oxopropan-2-yl)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/132201

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물alpha-Bromo-2-nitrotolueneHCID 77569—
반응물tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylateHCID 1514280—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 4-(1-methoxy-3-(2-nitrophenyl)-1-oxopropan-2-yl)piperidine-1-carboxylateHCID 5973204141%

반응 조건

온도-78 °C

반응 단계

tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate (240 mg, 0.93 mmol) was dissolved in tetrahydrofuran (7 mL). Mixture was cooled to −78° C. A 0.5 M solution of potassium bistrimethylsilyl)amide in toluene (2.2 mL, 1.1 mmol) was added to the mixture drop-wise. Reaction stirred at −78° C. for 20 minutes. A solution of 2-nitrobenzylbromide (240 mg, 1.1 mmol) in tetrahydrofuran (2 mL) was added to the reaction mixture drop-wise. Reaction stirred at −78° C. for 40 minutes. Dry ice bath was removed and the reaction mixture was allowed to warm to room temperature over 30 minutes. Reaction was quenched with aqueous ammonium chloride. Mixture was extracted with ethyl acetate (2×20 mL). Combined extracts were dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography afforded the title compound as yellow oil in 41% yield. MS m/e (M−C4H8+H)+=337.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384930B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-fbefab7c72394e35b4538b0b37dec6d6
출처 메모uspto-grants-2008_06