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HRID 844374생성일: 2026년 10월 25일

5-(2-Nitroethenyl)-1,3-benzodioxole → Methyl 2-(4-hexenoyl)-4-nitro-3-(1,3-benzodioxole-5-yl)butyrate

https://huagongshe.com/reaction/844374

반응식

참여 물질

역할이름HCID투입량
반응물5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 94945—
반응물6-Octenoic acid,3-oxo-, methyl esterHCID 5128463—
반응물Ethyl acetate hexaneHCID 21226206—
촉매1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
용매IsopropanolHCID 3776—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-(4-hexenoyl)-4-nitro-3-(1,3-benzodioxole-5-yl)butyrateHCID 5395966782%

반응 단계

A solution of methyl 3-oxo-6-octenoate (502 mg, 2.95 mmol) in 10 mL of isopropanol was added to a solution of 5-(2-nitrovinyl)-1,3-benzodioxole (712 mg, 3.69 mmol) in 10 mL THF, then DBU (22 μL, 0.15 mmol) was added. The resulting reddish solution was stirred at room temperature for 20 minutes. TLC (ethyl acetate-hexane, 1:3) indicated complete consumption of ketoester. The solution was concentrated in vacuo and flash chromatographed on silica gel eluting with 18% ethyl acetate in hexane to produce 879 mg (2.42 mmol, 82%) of the title compound as a mixture of diastereomers in a 1:1 ratio. 1H NMR (CDCl3, 300 MHz) 61.55-1.66 (m, 3H), 2.02-2.17 (br m, 1H), 2.20-2.37 (m, 1.5H), 2.49-2.76 (m, 1.5H), 3.57 (s, 1.5H), 3.74 (s, 1.5H), 3.97 (d, J=7.5H, 0.5H) and 4.05 (d, J=8 Hz, 0.5H), 4.10-4.20 (m, 1H), 4.68-4.82 (m, 2H), 5.06-5.52 (m, 2H), 5.95 (2s, 2H), 6.65 (m, 1H), 6.68 (dr s, 1H), 6.75 (d, 7.5 Hz, 1H). MS (DCl/NH3) m/e 381 (M+NH4)+. Anal calcd for C18H21NO7: C, 59.50; H, 5.82; N, 3.85. Found: C, 59.32; H, 5.71; N, 3.72.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06380241B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-ee3a38d926694eed8a3b627573520538
출처 메모uspto-grants-2002_04