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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750056Generated: November 2, 2026

Ammonia → HCID 86708231, compound

https://huagongshe.com/reaction/1750056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethylamineHCID 6329—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium pentafluoropropionateHCID 2733305—
Reactant2-Chloro-5-iodopyridineHCID 4397176—
CatalystCopper iodideHCID 83717—
SolventO-XyleneHCID 7237—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86708231HCID 86708231—

Reaction Conditions

Temperature150 °C

Reaction Steps

28 g of sodium pentafluoropropionate and 14 g of copper iodide were added to a mixture of 7.2 g of 2-chloro-5-iodopyridine, 75 ml of NMP and 75 ml of xylene under room temperature, and the mixture was heated to 150° C. and heated and stirred for 5.5 hours. After cooling the mixture to 80° C., 180 ml of an aqueous methylamine solution (40%) was added in 4 parts every 2 hours, and the mixture was heated and stirred for 8.5 hours. After the reaction, the mixture was ice-cooled to 0° C, a 28% aqueous ammonia solution and a saturated aqueous sodium bicarbonate solution were added, and the mixture was extracted with methyl tert-butyl ether (hereinafter, referred to as MTBE). The combined organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was applied to a silica gel column chromatography to obtain 4.6 g of methyl-(5-pentafluoroethyl-pyridin-2-yl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156838B2
Source datasetuspto-grants-2015_10
ORD IDord-74986d6f50054eff9f88e4f3020022d5
Source noteuspto-grants-2015_10