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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65471Generated: October 25, 2026

Benzene, (3-chloro-1-propenyl)- → 1-(Vinylbenzyl)-3-((S)-alpha-methylbenzylcarbamoyl)-pyridinium chloride

https://huagongshe.com/reaction/65471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, (3-chloro-1-propenyl)-HCID 94242—
ReactantN-((S)-alpha-methylbenzyl)nicotinamideHCID 765754—
SolventMethanolHCID 887—
Product1-(Vinylbenzyl)-3-((S)-alpha-methylbenzylcarbamoyl)-pyridinium chlorideHCID 7045186789.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 100 ml methanol solution containing 2.26 g (1.00×10-2 mols) of N-((S)-α-methylbenzyl)nicotinamide was charged into a 250 ml round bottom flask equipped with condenser, addition funnel, drying tube, nitrogen purge and magnetic stirrer. To this stirred reaction mixture was added, dropwise over a 10 minute interval, 50 ml of a methanol solution containing 1.53 g (1.00×10-2 mols) of chloromethylstyrene. The solution was stirred for 24 hours at 25° C., then was concentrated under vacuum to afford solid which was recrystallized from methanol to yield 3.40 g (8.98×10-3 mols) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614770
Source datasetuspto-grants-1986_09
ORD IDord-5f8417b8409e4cb6abf2aaa05ff224db
Source noteuspto-grants-1986_09