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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421932Generated: November 2, 2026

Triethylamine → HCID 11949616, compound

https://huagongshe.com/reaction/2421932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
ReactantHCID 63317696HCID 63317696—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11949616HCID 1194961632.4%

Reaction Steps

To 0.06 g of 2-(5-bromopyrimidin-2-yl)ethanamine (3.0 mmol) and triethylamine (0.03 g, 1.0 equivalent) in THF (5 ml), at room temperature whilst stirring, was added the 2-trifluoromethyl benzoyl chloride (0.062 g, 1.0 equivalent) and the mixture was left to stir at room temperature overnight. The solvent was removed by evaporation in vacuo and saturated sodium bicarbonate (10 mls) was added. The mixture was extracted with dichloromethane and the organic phase was collected, dried over MgSO4, and evaporated in vacuo to give the crude product which was purified by chromatography on silica using 1:1 heptane/ethyl acetate to yield to 0.036 g of N-[2-(5-bromopyrimidin-2-yl)ethyl]-2-(trifluoromethyl)benzamide (Compound A-1) (32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960391B2
Source datasetuspto-grants-2011_06
ORD IDord-e3a87bdb6ccb47abae1c73fd50e3d20b
Source noteuspto-grants-2011_06