HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718157Generated: October 27, 2026
Pyridine → ethyl N-ethoxycarbonyl-2-methoxyacetimidate
https://huagongshe.com/reaction/718157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ethyl 2-methoxyethanecarboximidate hydrochloride | HCID 12816254 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl N-ethoxycarbonyl-2-methoxyacetimidate | HCID 90426579 | 102.6% |
Reaction Steps
Ethyl 2-methoxyacetimidate hydrochloride (0.95 g, 6.18 mmol) was suspended in DCM (12.4 mL) and the mixture was cooled to 0° C. Pyridine (2.5 mL, 30.9 mmol) and ethyl chloroformate (1.2 mL, 12.4 mmol) were added sequentially and the solution was allowed to warm to RT and stirred for 12 h. EtOAc (100 mL) was added and solids were removed by filtration through a pad of diatomaceous earth. The filtrate was concentrated in vacuo to afford ethyl N-ethoxycarbonyl-2-methoxyacetimidate (1.2 g, 100%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 4.08-4.03 (m, 2H), 3.90 (q, J=7.0 Hz, 4H), 3.20 (s, 3H), 1.11 (t, J=6.9 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193719B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-016e56860629486287be1f3e1f7ef90b |
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| Source note | uspto-grants-2015_11 |
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