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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Reactant | N-((S)-alpha-methylbenzyl)nicotinamide | HCID 765754 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(Vinylbenzyl)-3-((S)-alpha-methylbenzylcarbamoyl)-pyridinium chloride | HCID 70451867 | 89.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04614770 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-5f8417b8409e4cb6abf2aaa05ff224db |
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| Source note | uspto-grants-1986_09 |
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