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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821968Generated: October 30, 2026

Pyridine → HCID 10413781, compound

https://huagongshe.com/reaction/1821968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 178513356HCID 178513356—
SolventTolueneHCID 1140—
ProductHCID 10413781HCID 10413781—

Reaction Steps

100 mg of 4-{3-[2,6-dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propoxy}-N-hydroxybenzamidine are placed in 2 ml of toluene. 20 mg of acetyl chloride and 2 ml of pyridine are added, and heating is carried out for 4 hours at 120° C. The reaction mixture is concentrated, and the residue is taken up in ethyl acetate and washed with dilute hydrochloric acid and water. Concentration of the organic phase and purification over silica gel yield the title compound (compound 1.10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608631B2
Source datasetuspto-grants-2009_10
ORD IDord-981467b986bb488bb9b8b6ad9ecc7305
Source noteuspto-grants-2009_10