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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240576Generated: November 1, 2026

N-Allylbenzylamine → 3-(Allyl-benzyl-carbamoyl)-but-3-enoic acid methyl ester

https://huagongshe.com/reaction/2240576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-AllylbenzylamineHCID 521150—
Reactant2-Methylene-succinate 4-methyl esterHCID 6994944—
ReactantEthylcarbodiimideHCID 12973440—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product3-(Allyl-benzyl-carbamoyl)-but-3-enoic acid methyl esterHCID 5744341449%

Reaction Steps

587 mg of 2-methylene-succinate 4-methyl ester (4.07 mM), 781 mg of 143-(dimethylamino)propyl]-3-ethylcarbodiimide (4.07 mM) and 75 mg of 4-(dimethylamino)pyridine (0.61 mM) were added to the reaction solution containing 300 mg of allylbenzylamine (2.04 mM) dissolved in methylene chloride solution (0.5M) with stirring for 10 hrs at room temperature. After the resulting mixture was washed with 5% HCl solution (10 ml), the mixture was diluted with ethyl acetate, washed with 10 ml of solution mixture mixed with saturated NaHCO3 solution and saturated NaCl solution to separate into an organic layer and water layer. The organic layer was dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resultant was purified by Silica gel column chromatography with a solvent mixture mixed with EtOAc and hexanes (1:1) as an eluant to give 272 mg of 3-(allyl-benzyl-carbamoyl)-but-3-enoic acid methyl ester (o) (yield: 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723376B2
Source datasetuspto-grants-2010_05
ORD IDord-3c8b318c324f43ff9c3c7f2f65eb43f6
Source noteuspto-grants-2010_05