HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132217Generated: October 23, 2026
Triethylamine → N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide
https://huagongshe.com/en/reaction/132217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 3-Pyridinecarboxaldehyde, 2-amino- | HCID 737633 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide | HCID 736837 | 90% |
Reaction Steps
Triethlyamine (7.6 mL, 54 mmol), was added to a solution of 2-aminopyridine-3-carboxaldehyde (4.45 g, 36 mmol) in dichloromethane (70 mL). Mixture was cooled to 0° C. A solution of pivaloyl chloride (5.3 mL, 43 mmol) in dichloromethane (30 mL) was added to the mixture. Reaction was warmed to room temperature. Mixture stirred at room temperature for 63 hours. Mixture was washed successively with water (2×50 mL) and brine (30 mL). Organic layer was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography afforded the title compound as off-white solid in 90% yield. (M+H)+=207.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384930B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-20ae7364aea64bc39f849fc707d69485 |
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| Source note | uspto-grants-2008_06 |
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