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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094447Generated: October 31, 2026

Tert-Butylamine → HCID 32217502, compound

https://huagongshe.com/reaction/1094447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-tert-Butyl-2-methyl-6-trifluoromethyl-nicotinic acidHCID 66639559—
SolventThionyl ChlorideHCID 24386—
ProductHCID 32217502HCID 32217502—

Reaction Steps

N-tert-Butyl-2-methyl-6-trifluoromethyl-nicotinic acid (5.0 g, 24 mmol) is refluxed in 10 mL of thionyl chloride for 3 h and is then concentrated under reduced pressure. The residue is dissolved in toluene and the solvent is removed under reduced pressure. The residue is again dissolved in toluene and the solvent is removed under reduced pressure. The resultant residue is dissolved in 50 mL of dichloromethane and to the solution is added tert-butyl amine (3.8 mL, 49 mmol) and triethylamine (6.8 mL, 49 mmol) and the reaction is allowed to stir overnight. The reaction is then poured into sat. ammonium chloride and extracted three times with dichloromethane. The combined organic phases are then washed with sat. NaHCO3, and brine. The organic layer is then dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford the title compound. Further purification is achieved by trituration from diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133907B2
Source datasetuspto-grants-2012_03
ORD IDord-c7774e2ba8794215b7d2b9e00bc03257
Source noteuspto-grants-2012_03