HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680441Generated: October 30, 2026
Sodium borohydride → 5-Benzylaminopyridine-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1680441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Benzylideneaminopyridine-2-carboxylic acid methyl ester | HCID 53671695 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Benzylaminopyridine-2-carboxylic acid methyl ester | HCID 54433419 | — |
Reaction Steps
The solution of 24.9 g of 5-benzylideneaminopyridine-2-carboxylic acid methyl ester in 70 ml of hot dimethylformamide is added all at once to the solution of 7.0 g of sodium borohydride in 300 ml of methanol while stirring at -20° C. The temperature of the reaction mixture raises spontaneously to 20° and is lowered to 0° by cooling. After 2 hours the mixture is warmed to room temperature for 15 minutes to ensure complete reaction. Approximately 1/2 of the methanol is distilled off, the concentrate is cooled to 0° and 3 ml of acetic acid and the solution of 12 ml of 12 N hydrochloric acid in 100 ml ice water is added. A precipitate begins to separate and 200 ml more ice water are added. After 30 minutes the precipitate is collected and washed well with water and recrystallized from acetonitrile, to yield the 5-benzylaminopyridine-2-carboxylic acid methyl ester, melting at 104°-107°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04273779 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-d17de7c9b5c34288bd205f4962f27772 |
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| Source note | uspto-grants-1981_06 |
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