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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3003생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/3003

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) δ 1.55-1.66 (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 (br 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 번호US05731434
출처 데이터셋uspto-grants-1998_03
ORD IDord-a43f21651da24fe980f402c4a2514be5
출처 메모uspto-grants-1998_03