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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612043Generated: October 31, 2026

Pyridine → HCID 22252930, compound

https://huagongshe.com/reaction/1612043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 178510673HCID 178510673—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 22252930HCID 2225293028.6%

Reaction Steps

To the solution of 1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfenyl-5-hydroxypyrazole (7.00 g, 16.6 mmol) and pyridine (4.91 g, 62.1 mmol) in 1,2-dichloroethane at room temperature was added trimethylacetyl chloride (4.37 g, 36.2 mmol) dropwise. Ice bath was used to maintain the temperature of the reaction. After 20 hr at room temperature, the organic layer was washed five times with aqueous KHSO4 till the aqueous solution was at pH 1. The organic layer was then dried (MgSO4) and concentrated to give a solid residue. Upon chromatographic purification via silica gel column of the solid residue, after trituration with pentane, a off-white solid (2.403 g, 28.6% yield, 97.0% HPLC purity) was provided as the desired product, m. p. 82–83 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992099B2
Source datasetuspto-grants-2006_01
ORD IDord-6c7f834fd1e14e6584e2d845ae15bc54
Source noteuspto-grants-2006_01