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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274675Generated: October 30, 2026

Triethylamine → HCID 20093314, compound

https://huagongshe.com/reaction/274675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 86748461HCID 86748461—
SolventDichloromethaneHCID 6344—
ProductHCID 20093314HCID 2009331460.7%

Reaction Steps

To a solution of 7.27 g (28.1 mmol) 4-[3-(N-benzylaminopropylthio)pyridine and 4.70 ml (33.7 mmol) of triethylamine in 150 ml of methylene chloride, 4.76 ml (33.7 mmol) of trifluoroacetic anhydride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/hexane=2:1 to 1:1) to obtain 6.04 g of 4-[3-(N-benzyl-N-fluoroacetylamino)-propylthio]pyridine (yield: 60.7% yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-f9d12759410c46e483a652ad99056f62
Source noteuspto-grants-1995_02