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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Carbonate | HCID 12021 | — |
| Edukt | 3-Amino-4-picoline | HCID 137935 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl N-(4-methylpyridin-3-yl)carbamate | HCID 11672725 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08461328B2 |
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| Quelldatensatz | uspto-grants-2013_06 |
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| ORD ID | ord-9d5cd1ef7c374d5e89d959be79315aa3 |
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| Quellennotiz | uspto-grants-2013_06 |
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