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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799454Generated: November 2, 2026

Cyanoacetic acid → N-(4-Chloro-benzyl)-2-cyano-acetamide

https://huagongshe.com/reaction/1799454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
Reactant4-ChlorobenzylamineHCID 66036—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-Chloro-benzyl)-2-cyano-acetamideHCID 69067389%

Reaction Steps

According to the Scheme 1 Step 1: A mixture of 4-chlorobenzylamine (10.0 g, 71 mmol), cyanoacetic acid (6.13 g, 72 mmol), HOBt (11 g, 72 mmol), EDCI.HCl (20 g, 106 mmol) in 100 mL of dioxane was stirred for 3 h at room temperature. The solvent was removed under vacuum and 300 mL of DCM was added. The organic layer was successively washed with 2×100 mL of water, 2×50 mL of a solution 1N of NaOH, 4×100 mL of water until neutral pH. The organic layer was dried over Na2SO4, filtered and concentrated to afford N-(4-chlorobenzyl)-2-cyanoacetamide 1(A) (13.12 g, 89%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344138B2
Source datasetuspto-grants-2013_01
ORD IDord-afcc915de2724649abbf182c11164c08
Source noteuspto-grants-2013_01