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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244159Generated: October 31, 2026

2-Cyanoacetyl chloride → HCID 69607367, compound

https://huagongshe.com/reaction/1244159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyanoacetyl chlorideHCID 11051594—
ReactantHCID 69607355HCID 69607355—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 69607367HCID 69607367—

Reaction Steps

2-Amino-4-styryl-thiophene-3-carboxylic acid ethyl ester (0.1298 g, 0.475 mmol) S was dissolved in anhydrous CH2Cl2 (2.0 mL). This was treated with cyanoacetyl chloride (0.713 mL, 0.713 mmol, 1 M in CH2Cl2) and stirred at room temperature for 1 hr. More cyanoacetyl chloride (0.238 mL, 0.238 mmol) was added and stirring was continued at room temperature for 1 hr then refluxed for 30 min. The reaction was diluted with EtOAc (25 mL). This was washed with sat. NaHCO3 (1×25 mL), H2O (1×25 mL), and brine (1×25 mL). The organic layer was dried (Na2SO4), filtered and the solvent removed in vacuo to give 0.0803 g (50%) of crude 7 which was carried on to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119205B2
Source datasetuspto-grants-2006_10
ORD IDord-7f77a490a7fc4ac2906a5a0bfacaa1f1
Source noteuspto-grants-2006_10