HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087094Generated: November 2, 2026
Sodium Hydroxide → 5-(Aminomethyl)-2-chloropyridine
https://huagongshe.com/reaction/1087094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | 58.1% |
Reaction Steps
A mixture of 14.99g of 2-chloro-5-(chloromethyl) pyridine, 63.01g of 25% ammonia water and 60ml of acetonitrile in a stainless steel autoclave was stirred for 2 hours in an oil bath of 80° C. After adding 12.3g of 30% sodium hydroxide aqueous solution, the reaction mixture was concentrated. The residue to which 200ml of ethanol were added was dried over anhydrous magnesium sulfate and, filtered to remove insoluble materials. The filtrate was concentrated and purified by a column chromatography [developing solvent: dichloromethane-methanol (4:1)] to afford 7.66g of 5-(aminomethyl)-2- chloropyridine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034404 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-42613b3047a549fe8e068f616e772585 |
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| Source note | uspto-grants-1991_07 |
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