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HRID 54570作成日:2026年10月24日

Toluene → Ethyl 2-(4-methoxybenzoyl)-4-nitromethyl-3-(1,3-benzodioxole-5-yl)butyrate

https://huagongshe.com/ja/reaction/54570

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ethyl AcetateHCID 8857—
反応物Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
反応物5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 94945—
触媒1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-(4-methoxybenzoyl)-4-nitromethyl-3-(1,3-benzodioxole-5-yl)butyrateHCID 22322609—

反応条件

温度80 °C

反応手順

To ethyl (4-methoxybenzoyl)acetate (23.0 g, 0.104 mol), prepared by the method of Krapcho et al., Org. Syn. 47, 20 (1967), and 5-(2-nitrovinyl)-1,3-benzodioxole (17.0 g, 0.088 mol) dissolved in 180 mL of toluene and heated to 80° C. was added 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU, 0.65 g) with stirring. The mixture was heated until all the nitro starting material dissolved. The solution was stirred without heating for 30 minutes and then an additional 0.65 g of DBU was added. After stirring an additional 45 minutes, thin layer chromatography (5% ethyl acetate in methylene chloride) indicated the absence of nitro starting material. Toluene (200 mL) was added, and the organic phase was washed with dilute hydrochloric acid and NaCl solution. The organic phase was dried over sodium sulfate and then concentrated under reduced pressure. The residue obtained was chromatographed on silica gel eluting with 3:1 hexane-ethyl acetate to give 21.22 g of the desired product as a mixture of isomers and 9.98 g. of recovered ethyl (4-methoxybenzoyl)acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622971
出典データセットuspto-grants-1997_04
ORD IDord-19a1f02e2a9c4cf59ae0b3f37bc6aeab
出典メモuspto-grants-1997_04