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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1257624Erstellt: 27. Oktober 2026

Dimethyl Carbonate → Methyl N-(4-methylpyridin-3-yl)carbamate

https://huagongshe.com/reaction/1257624

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl CarbonateHCID 12021—
Edukt3-Amino-4-picolineHCID 137935—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl N-(4-methylpyridin-3-yl)carbamateHCID 1167272562%

Reaktionsschritte

A solution of potassium tert-butoxide (32.8 g, 277 mmol) in THF (250 mL) at 0° C. was treated with 3-amino-4-methylpyridine (10.0 g, 92.5 mmol) and the resulting mixture stirred for 30 minutes before dimethyl carbonate (11.7 mL, 139 mmol) was added. The mixture was stirred for 30 minutes then quenched with water and extracted with ethyl acetate. The combined organic phases were washed with brine then dried over sodium sulfate and concentrated under vacuum. The resulting residue was purified by column chromatography on silica gel (DCM) then triturated with diethyl ether to afford 9.42 g (62%) of (4-methyl-pyridin-3-yl)-carbamic acid methyl ester. LCMS (Method B, ESI): RT=0.40 min, m+H=167.4; 1H NMR (400 MHz, CDCl3) δ: 8.86 (s, 1H), 8.28 (d, 1H), 7.12-7.12 (m, 1H), 6.45 (s, 1H), 3.80 (s, 3H), 2.28 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08461328B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-9d5cd1ef7c374d5e89d959be79315aa3
Quellennotizuspto-grants-2013_06