HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017707Generated: October 30, 2026
Dimethylformamide → tert-butyl N-(3-formylpyridin-2-yl)carbamate
https://huagongshe.com/reaction/1017707
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-(Boc-amino)pyridine | HCID 11206349 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-butyl N-(3-formylpyridin-2-yl)carbamate | HCID 14177125 | — |
Reaction Steps
tert-Butyllithium (1.7 M, 14.5 mL, 24.6 mmol, 2.39 equiv) was added to a solution of pyridin-2-yl-carbamic acid tert-butyl ester (5-1, 2.00 g, 10.3 mmol, 1 equiv) in ethyl ether (100 mL) at −78° C., and the resulting mixture was warmed to 0° C. and stirred for 1 h. N,N-Dimethylformamide (8.00 mL, 103 mmol, 10.0 equiv) was added with rapid stirring. The mixture was stirred at 0° C. for 10 min, then partitioned between half-saturated aqueous ammonium chloride solution (100 mL). The aqueous layer was further extracted with ethyl acetate (100 mL), and the combined organic layers were dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (40% ethyl acetate in hexanes) to afford (3-formyl-pyridin-2-yl)-carbamic acid tert-butyl ester (5-2) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479512B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-2b6774d61de4477ba679acdc8cef5df7 |
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| Source note | uspto-grants-2002_11 |
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