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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485196Generated: October 29, 2026

Methane → HCID 15592370, compound

https://huagongshe.com/reaction/485196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPivaloyl chlorideHCID 62493—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantHCID 178418361HCID 178418361—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15592370HCID 15592370—

Reaction Steps

To an ice-cooled solution of 45 g (0.35 mole) of 5-amino-2-chloropyridine and 42.4 g (0.42 mole) of triethylamine in 300 ml of CH2Cl2 was added, dropwise, a solution of 44.3 g (0.368 moles) of trimethyl acetyl chloride in 60 ml of dichloromethane over a period of 1.5 hours. This mixture was stirred at room temperature for 2 hours, poured into 5% aqueous NaOH and the dichloromethane layer separated. The organic layer was washed with 5% aqueous NaOH, dried over Na2SO4 and evaporated to leave a brown oil which solidified on standing. This solid was taken up in hot ethyl acetate, treated with charcoal, filtered and diluted with hexane. Cooling this solution resulted in the precipitation of 58.7 g (79% of theoretical) of white crystals having a melting point of 120°-123° C. Carbon, hydrogen and nitrogen content calculated for C10H13ClN2O is C, 56.47; H, 6.16; and N, 13.17 percent by weight which compared to that actually found of C, 56.31; H, 6.14; and N, 13.02 percent by weight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536208
Source datasetuspto-grants-1985_08
ORD IDord-e1e16fd6b1ef4f1e96b30edb6804da4e
Source noteuspto-grants-1985_08