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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479929Generated: November 3, 2026

Pyridine → HCID 22177449, compound

https://huagongshe.com/reaction/479929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3,5-Dinitrobenzoyl chlorideHCID 7432—
Reactant11-Bromo-1-undecanolHCID 74163—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 22177449HCID 2217744990%

Reaction Conditions

Temperature0 °C

Reaction Steps

11.4 g (45.4 mmol) 11-bromo-1-undecanol, 11.0 g (47.7 mmol) 3,5-dinitrobenzoyl chloride, 54 mg 4-dimethylaminopyridine were dissolved in 94 ml dichloromethane. The solution was subsequently cooled to 0° C. and then 18.3 ml (227 mmol) Pyridine was added dropwise, in the course of 25 minutes. After 4.5 hours at 0° C. the reaction mixture was partitioned between dichloromethane and water; the organic phase was washed repeatedly with water, dried over sodium sulfate, filtered and concentrated by rotary evaporation. Chromatography of the residue on 200 g silica gel using Toluene yielded 18.1 g (90%) 3,5-Dinitrobenzoic acid 11-bromoundecyl ester as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649230B1
Source datasetuspto-grants-2003_11
ORD IDord-bcc822fa02c446efb488c6f3c784c5fe
Source noteuspto-grants-2003_11