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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1599098생성일: 2026년 10월 27일

Benzoyl chloride, 3-nitro- → Tert-butyl 3-nitrobenzoate

https://huagongshe.com/reaction/1599098

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chloride, 3-nitro-HCID 8495—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 3-nitrobenzoateHCID 1196136963.5%

반응 단계

Potassium t-butoxide solid (3.82 g, 32.30 mmol) was added to a solution of 3-nitrobenzoyl chloride (5.00 g, 26.94 mmol) in dry tetrahydrofuran (70 mL) and stirred under nitrogen for 2 hrs. The reaction mixture was concentrated in vacuo and partitioned between dichloromethane and water. After separating the phases, the aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, dried over anhydrous magnesium sulfate, filtered and then concentrated in vacuo. The crude product was purified on flash grade silica gel using 0-5% gradient of ethyl acetate in n-hexane. Fractions containing the product were combined, concentrated in vacuo, and then dried under high vacuum to provide 3.82 g of the title compound as an oil. 1H NMR (300 MHz, CDCl3) d 8.79 (m, 1H), 8.35 (m, 2H), 7.62 (m, 1H), 1.63 (s, 9H); low resolution MS (Cl) m/e 224 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05739129
출처 데이터셋uspto-grants-1998_04
ORD IDord-3ba72393137a4e0d8e5cddb209939684
출처 메모uspto-grants-1998_04