HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164656Generated: October 31, 2026
4-Nitrobenzyl bromide → 2-(Benzylsulfanyl)-1-[(4-nitrophenyl)methyl]pyridin-1-ium bromide
https://huagongshe.com/reaction/1164656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | 2-benzylsulfanylpyridine | HCID 472961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Benzylsulfanyl)-1-[(4-nitrophenyl)methyl]pyridin-1-ium bromide | HCID 13435003 | — |
Reaction Steps
A mixture of 4-nitrobenzyl bromide (1.08 g) and 2-(benzylthio)pyridine (1.05 g) were heated at 100° C. for 4 hours and cooled. Crystals which formed on trituration with acetone were removed by filtration and dried to give the title compound as a quarter hydrate (1.6 g) mp 160°-2° C. (Found C, 53.8; H, 4.5; N, 6.4%. C19H17BrN2O2S1/4H2O requires C, 54.1; H, 4.2; N, 6.6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04370477 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-ab26f00d6e0d4bc09df041ae57b4f64f |
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| Source note | uspto-grants-1983_01 |
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