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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482340생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/482340

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 (3.82 g, 32.30 mmol) is added to a solution of 3-nitrobenzoyl chloride (5.00 g, 26.94 mmol) in anhydrous THF (70 mL) and stirred under nitrogen for 2 hrs. The reaction mixture is concentrated in vacuo and partitioned between DCM and water. After separating the phases, the aqueous layer is back-extracted with ethyl acetate. The organic layers are combined, dried over anhydrous magnesium sulfate, filtered and then concentrated in vacuo. The crude product is purified on flash grade silica gel using 0-5% gradient of ethyl acetate in n-hexane. Fractions containing the product are combined, concentrated in vacuo, and then dried under high vacuum to provide the title compound as an oil (3.82 g, 17.1 mmol). 1H NMR (300 MHz, CDCl3) δ=1.63 (s, 9H); 7.62 (t, J=7.9 Hz, 1H); 8.29-8.41 (m, 2H); 8.78-8.80 (m, 1H). MS (Cl): [M+H]+ =224.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05795887
출처 데이터셋uspto-grants-1998_08
ORD IDord-be1c5ba31c0b42b58399cd0d291adb63
출처 메모uspto-grants-1998_08