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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718157Generated: October 27, 2026

Pyridine → ethyl N-ethoxycarbonyl-2-methoxyacetimidate

https://huagongshe.com/reaction/718157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl 2-methoxyethanecarboximidate hydrochlorideHCID 12816254—
SolventDichloromethaneHCID 6344—
Productethyl N-ethoxycarbonyl-2-methoxyacetimidateHCID 90426579102.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193719B2
Source datasetuspto-grants-2015_11
ORD IDord-016e56860629486287be1f3e1f7ef90b
Source noteuspto-grants-2015_11