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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250339Generated: October 31, 2026

Pyridine → 2-Bromoethyl 4-nitrobenzoate

https://huagongshe.com/reaction/1250339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantEthanol, 1-bromo-HCID 14202443—
Product2-Bromoethyl 4-nitrobenzoateHCID 280396—

Reaction Steps

Under a nitrogen atmosphere, bromoethanol (29 mmols) was dissolved in 25 mL ether. Pyridine (34 mmols) was added to the solution, followed by a solution of 4-nitrobenzoyl chloride (27 mmols) in 35 mL ether. The reaction was stirred overnight, and a white precipitate was formed. Ether (50 mL) was added, and the reaction mixture was then washed with aqueous KHSO4, aqueous NaHCO3, and water. The ether layer was then dried over Na2SO4, filtered, and concentrated to give 6.3 g of 4-nitrobenzoic acid 2-bromo-ethyl ester. Material was used in coupling reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337423B1
Source datasetuspto-grants-2002_01
ORD IDord-6ab78bdfa16b49f1b0686d674ff20e5f
Source noteuspto-grants-2002_01