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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496753Generated: October 25, 2026

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

https://huagongshe.com/reaction/496753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
ReactantBenzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
Reactant5-(2-Nitroethenyl)-1,3-benzodioxoleHCID 94945—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(4-methoxybenzoyl)-4-nitromethyl-3-(1,3-benzodioxole-5-yl)butyrateHCID 22322609—

Reaction Conditions

Temperature80 °C

Reaction Steps

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 (min) 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946481B1
Source datasetuspto-grants-2005_09
ORD IDord-a558280064cc45938c923dd66c1c888e
Source noteuspto-grants-2005_09