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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655544Generated: October 30, 2026

Triethylamine → HCID 67079909, compound

https://huagongshe.com/reaction/655544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-(Pyridin-3-yl)anilineHCID 459521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67079909HCID 6707990968%

Reaction Steps

A solution of 3-pyridin-3-ylaniline (500 mg, 2.94 mmol) in tetrahydrofuran (6 mL) was added at room temperature to a solution of phenyl chloroformate (450 mg, 2.94 mmol), then triethylamine (288 mg, 2.84 mmol) was added. After 15 min the reaction mixture was concentrated under vacuum, then the residue was partitioned between ethyl acetate and 1 M aq. sodium hydrogencarbonate solution. The organic layer was dried (MgSO4) and evaporated. The residue was taken up in tetrahydrofuran (1 mL), then heptane (10 mL) was added. The slurry was stirred for 30 min, then the precipitate was collected by filtration to afford the title compound (566 mg, 68%). Off-white solid, MS (ISP)=291.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071586B2
Source datasetuspto-grants-2011_12
ORD IDord-482a700840964cf99f32efb8f20bdbf3
Source noteuspto-grants-2011_12