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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180642Generated: November 1, 2026

Methyl cyanoacetate → HCID 86612866, compound

https://huagongshe.com/reaction/1180642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl cyanoacetateHCID 7747—
ReactantAcetic AnhydrideHCID 7918—
Reactant179802-16-5HCID 11052183—
CatalystZincchlorideHCID 3007855—
ProductHCID 86612866HCID 86612866—

Reaction Conditions

Temperature110 °C

Reaction Steps

Into a dried 3L three neck-round bottom flask with a stirrer bar, nitrogen-inlet, thermocouple and a addition funnel were charged 150 g (851.26 mmol) 3-(dimethoxymethyl)-2-methoxyoxolane, 355.27 g (3.48 mol) Ac2O and 2.12 g (15.55 mmol) ZnCl2 and the mixture was heated for 1.25-1.5 h at 100-120° C. to reflux. The solution started to become brown and a small portion of solvent was distilled off at atmospheric pressure. To the reaction mixture 76.7 g (774 mmol) methylcyanacetate was slowly added over 1 h while continuing to distill off solvent. After the addition was completed, the reaction mixture was evacuated and the residual solvent was distilled off. The residue was treated with 224 g MeOH and again evacuated and the solvent was distilled off. The residual black oil was charged with 500 ml CH2Cl2 and washed twice with 500 ml water. The solvent was distilled off under reduced pressure and the residue was treated with a mixture of 350 ml MTBE and 285 ml heptane. The reaction mixture was heated to reflux at 55-60° C. for 1½ h, then cooled down to 0° C. and kept at 0° C. for 16 h. The crystals were filtered off and three times washed with cold 250 ml MTBE.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282583B2
Source datasetuspto-grants-2007_10
ORD IDord-4921d760e87b42aba5b78d9ffa1e601b
Source noteuspto-grants-2007_10