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HRID 983550作成日:2026年10月26日

Water → 1,4-Benzodioxin,2,3-dihydro-6-(2-nitroethenyl)-

https://huagongshe.com/reaction/983550

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物NitromethaneHCID 6375—
反応物2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
反応物Ammonium AcetateHCID 517165—
溶媒Acetic AcidHCID 176—
生成物1,4-Benzodioxin,2,3-dihydro-6-(2-nitroethenyl)-HCID 2415445161%

反応条件

温度110 °C

反応手順

To 1,4-benzodioxane-6-carboxaldehyde (10.0 g, 60 mmol) in acetic acid (50 mL) was added nitromethane (6.3 mL, 1.9 eq.) and ammonium acetate (5.1 g, 1.1 eq.). After heating at 110° C. for 4 hours the mixture was cooled to ambient temperature, water (150 mL) was added, and the solid precipitate was collected by filtration. The solid was crystallized from methylene chloride-hexane (1:1, 45 mL) to obtain 7.6 g (61%) of 6-(2-nitroethenyl)-1,4-benzodioxane. To a portion of the solid (3.58 g) dissolved in MeOH-EtOH-AcOEt (1:1:1, 450 mL) was added 10% Pd/C (1.7 g) and concentrated HCl (3.3 mL, 2.3 eq). After shaking on a Parr hydrogenator at 45 psi for 5 hours, the catalyst was removed by filtration through Celite and washed with methanol. Evaporation of the filtrate gave 3.59 g (96%) of 1,4-benzodioxan-6-ethanamine, hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06864263B2
出典データセットuspto-grants-2005_03
ORD IDord-f79c2bad938e429190c1d1673d5bc520
出典メモuspto-grants-2005_03