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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactanttert-Butyl (2-methoxypyridin-3-yl)carbamateHCID 11064075—
ReactantButyllithiumHCID 178418339—
ProductTert-butyl 2-methoxy-4-methylpyridin-3-ylcarbamateHCID 10082908—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532358
Source datasetuspto-grants-1996_07
ORD IDord-464c93e213e845d1a1af1f2b772bcfb8
Source noteuspto-grants-1996_07