HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258610Generated: November 1, 2026
Formic Acid → N-(6-Methylpyridin-2-yl)formamide
https://huagongshe.com/reaction/1258610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-6-methylpyridine | HCID 15765 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(6-Methylpyridin-2-yl)formamide | HCID 12857768 | 32% |
Reaction Steps
To stirred neat formic acid (3.83 mL, 101.7 mmol) was added acetic anhydride (6.98 mL, 74.0 mmol). The reaction mixture was heated under stirring at 70° C. for 2 hrs and allowed to room temperature. A solution of 6-methylpyridin-2-amine (5.00 g, 46.23 mmol) in tetrahydrofurane (30 mL), was added dropwise in order to prevent temperature from rising above 45° C. The reaction mixture was allowed to room temperature and stirred for further 1 hr. The reaction mixture was concentrated in vacuo and the residue was diluted in 100 mL of ethanol. The reaction mixture was stirred for 2 hrs at room temperature concentrated in vacuo, yielding to N-(6-methylpyridin-2-yl)formamide as a yellow solid [2.00 g, yield 32%; HPLC/MS: m/z=137 (M+H); logP(HCOOH)=0.45].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466176B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-d2e99765231c47cb9fba30d7098bbbb3 |
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| Source note | uspto-grants-2013_06 |
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