Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615485Generated: November 1, 2026

Pyridine → 5-chloro-N,N-diethyl-2-iodobenzamide

https://huagongshe.com/reaction/1615485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethylamineHCID 8021—
ReactantTetrahydrofuranHCID 8028—
Reactant5-Chloro-2-iodobenzoyl chlorideHCID 86601585—
Product5-chloro-N,N-diethyl-2-iodobenzamideHCID 6818295461%

Reaction Steps

In a 100 mL round bottomed flask was placed the 5-chloro-2-iodobenzoyl chloride prepared above. Pyridine (50 mL, 600 mmol) and tetrahydrofuran (10 mL, 100 mmol) were then added. To the reaction mixture was added diethylamine (3 mL, 30 mmol) and the mixture was stirred for 3 hr at rt. The mixture was stirred for an additional 3 hr at 50° C. The mixture was allowed to cool to rt and then concentrated under reduced pressure. The residue was dissolved in EtOAc (100 mL) and then washed with 1N HCl (50 mL×2), 1N NaOH (50 mL), brine (50 mL), and dried over anhydrous MgSO4. Insoluble materials were removed by filtration and the filtrate was concentrated under reduced pressure to obtain the title compound (1.96 g, 61%) as a light yellow syrup. LCMS: (FA) ES+ 338, 340; 1H NMR (300 MHz, d6-DMSO) δ ppm 7.86 (d, 1H), 7.38 (d, 1H), 7.21 (dd, 1H), 3.61-3.68 (m, 1H), 2.91-3.29 (m, 3H), 1.17 (t, 3H), 1.01 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765746B2
Source datasetuspto-grants-2014_07
ORD IDord-7b93011e94204a8487cc9a4c4717080b
Source noteuspto-grants-2014_07