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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301057Generated: November 2, 2026

Pyridine → HCID 22287130, compound

https://huagongshe.com/reaction/2301057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Acetoxyisobutyroyl chlorideHCID 123496—
Reactant2-Chloro-4-iodoanilineHCID 282930—
SolventDichloromethaneHCID 6344—
ProductHCID 22287130HCID 22287130—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

2-Chloro-4-iodoaniline (5 g) was dissolved in DCM (100 ml) and cooled to 0-5° C. in an ice bath. Pyridine (2.1 ml) was added followed by dropwise addition of 2-acetoxy-2-methylpropanoyl chloride (3.44 ml) and the mixture was allowed to warm to ambient temperature over 15 hours. The solvent was removed by evaporation and the residue was purified by flash chromatography eluting with 10-50% ethyl acetate/hexane to give the title compound (7.5 g) as a solid. Mp 156-158° C.; NMR (CDCl3): 1.7 (s. 6H), 2.2 (s, 3H), 7.6 (d, 1H), 7.7 (d, 1H), 8.2 (d, 1H), 8.4 (s, 1H); MS (ESP−): 380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498275B1
Source datasetuspto-grants-2002_12
ORD IDord-85a3f8044bc04993bfbafcd3b529f208
Source noteuspto-grants-2002_12