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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081535Generated: November 1, 2026

Benzyl Bromide → HCID 19769112, compound

https://huagongshe.com/reaction/2081535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantAluminumHCID 5359268—
ReactantHCID 19769113HCID 19769113—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
ProductHCID 19769112HCID 19769112—

Reaction Steps

To a partial suspension of 3-cyano-5-ethyl-6-benzyloxymethyl-2(1H)-pyridinone (1.36 g, 5.08 mmol) in dry benzene (20 mL) was added benzyl bromide (0.80 mL, 6.7 mmol) and then silver carbonate (1.43 g, 5.2 mmol). This mixture was covered with aluminum foil and allowed to stir at room temperature. After 24 hours, the reaction was estimated to be ~80% complete. Additional silver carbonate (0.40 g, 1.45 mmol) was added and the mixture was stirred for another 24 hours until complete. The silver salts were removed by filtration, rinsed with benzene and the combined benzene washings were evaporated to give the pure product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185251
Source datasetuspto-grants-1993_02
ORD IDord-3fea9745d05d4acb9bd5e99286fb2f27
Source noteuspto-grants-1993_02