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HRID 3003作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 94945—
反応物6-Octenoic acid,3-oxo-, methyl esterHCID 5128463—
反応物Ethyl acetate hexaneHCID 21226206—
触媒1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
溶媒IsopropanolHCID 3776—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(4-hexenoyl)-4-nitro-3-(1,3-benzodioxole-5-yl)butyrateHCID 5395966782%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731434
出典データセットuspto-grants-1998_03
ORD IDord-a43f21651da24fe980f402c4a2514be5
出典メモuspto-grants-1998_03