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HRID 3003Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 94945—
Edukt6-Octenoic acid,3-oxo-, methyl esterHCID 5128463—
EduktEthyl acetate hexaneHCID 21226206—
Katalysator1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 2-(4-hexenoyl)-4-nitro-3-(1,3-benzodioxole-5-yl)butyrateHCID 5395966782%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731434
Quelldatensatzuspto-grants-1998_03
ORD IDord-a43f21651da24fe980f402c4a2514be5
Quellennotizuspto-grants-1998_03