HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257624Generated: October 27, 2026
Dimethyl Carbonate → Methyl N-(4-methylpyridin-3-yl)carbamate
https://huagongshe.com/reaction/1257624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | 3-Amino-4-picoline | HCID 137935 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl N-(4-methylpyridin-3-yl)carbamate | HCID 11672725 | 62% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461328B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-9d5cd1ef7c374d5e89d959be79315aa3 |
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| Source note | uspto-grants-2013_06 |
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