HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412687Generated: October 26, 2026
Ethanol → Propanoic acid, 3-ethoxy-3-imino-, ethyl ester
https://huagongshe.com/reaction/412687
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Propanoic acid, 3-ethoxy-3-imino-, ethyl ester | HCID 75346 | 110.6% |
Reaction Steps
Ethyl cyanoacetate (8 mL, 75 mmol) in anhydrous benzene (100 mL) was combined under nitrogen with anhydrous ethanol (6 mL, 105 mmol). The mixture was cooled to 10° C. (ice/acetone) and bubbled 20 minutes with dry hydrogen chloride gas. The mixture was slowly warmed to room temperature, sealed and stirred for approximately 18 hours. The mixture was diluted with diethyl ether (400 mL) and let stand for 5 hours at room temperature to give a crystalline solid. The solid was isolated by filtration, washed several times with anhydrous diethyl ether and dried to provide ethyl 3-ethoxy-3-iminopropionate (13.2 g, 90% yield) as a colorless, crystalline solid; 1H-NMR (300 Mhz, CDCL3): 7.84 (d, 1H, J=10.0 Hz), 7.19-7.36 (m, 5H), 7.00-7.06 (m, 2H), 4.10 (t, 2H, J=5.7 Hz), 2.73 (t, 2H, J=6.5 Hz), 1.89 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562854B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-ac8807b3f6ea4531ac445c635a0b4252 |
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| Source note | uspto-grants-2003_05 |
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