HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724872Generated: October 31, 2026
Dimethylformamide → tert-Butyl 4-chloro-3-formylpyridin-2-ylcarbamate
https://huagongshe.com/reaction/1724872
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-butyl N-(4-chloropyridin-2-yl)carbamate | HCID 1516418 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 4-chloro-3-formylpyridin-2-ylcarbamate | HCID 46204204 | — |
Reaction Steps
Dissolve tert-butyl 4-chloropyridin-2-ylcarbamate (1.95 g, 0.00855 moles) in dry THF (50 mL) and cool to −78° C. under nitrogen atmosphere. Add dropwise 1.6 M n-BuLi/hexane (12.8 mL, 0.02053 moles) over a period of 15 minutes while maintaining the reaction temperature below −70° C. Stir the resulting red orange solution at −78° C. for 2 hours. Add DMF (3.3 mL, 0.04275 moles) dropwise to the reaction mixture while maintaining the reaction temperature below −70° C. Stir further at −78° C. for 2 hours and then quench the reaction mixture with saturated ammonium chloride (50 mL). Warm the reaction mixture to room temperature, extract with EtOAc (3×50 mL) and dry with MgSO4. Filter and concentrate under reduced pressure to afford a yellow viscous oil. Purify the crude product by flash column chromatography using 15-20% EtOAc/hexane to afford the title product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488740B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-b504d4fd05b54c95be18388f816a8c20 |
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| Source note | uspto-grants-2009_02 |
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