HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734120Generated: October 27, 2026
Diethyl Ether → Tert-butyl 2-methoxy-4-methylpyridin-3-ylcarbamate
https://huagongshe.com/reaction/1734120
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | tert-Butyl (2-methoxypyridin-3-yl)carbamate | HCID 11064075 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Tert-butyl 2-methoxy-4-methylpyridin-3-ylcarbamate | HCID 10082908 | — |
Reaction Steps
To a stirred solution of 1.12 g (5 mmol) of 3-(tert-butoxycarbonylamino)-2-methoxypyridine in 25 mL of dry ether containing 1.8 mL, (12 mmol) of TMEDA at -78° C. under an argon atmosphere was added 4.8 mL (12 mmol) of a 2.5M solution of nBuLi in hexanes. The mixture was then warmed to -10° C. for 2 h. Recooling to -78° C. and treatment with iodomethane (0.99 g, 7 mmol) followed by warming to room temperature for 1 h produced the desired product which was purified by quenching with water, washing the ether layer with 0.1N HCl, drying (MgSO4), concentration and flash chromatography (9:1 hexanes:EtOAc). Yield: 1.00 g (84%). Recrystallization from heptane provided further purification. m.p.: 93°-95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05532358 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-464c93e213e845d1a1af1f2b772bcfb8 |
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| Source note | uspto-grants-1996_07 |
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