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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376702Generated: October 30, 2026

Pyridine → HCID 22252930, compound

https://huagongshe.com/reaction/2376702

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 numberUS07468381B2
Source datasetuspto-grants-2008_12
ORD IDord-264df5cbd9184145ae062b2c5ea07cf2
Source noteuspto-grants-2008_12