HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602820Generated: October 30, 2026
Ethyl formate → Potassium 2-ethoxycarbonyl-2-(1-ethoxy-ethylideneamino)-ethenolate
https://huagongshe.com/reaction/602820
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Ethyl 2-(1-ethoxyethylideneamino)acetate | HCID 295983 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Potassium 2-ethoxycarbonyl-2-(1-ethoxy-ethylideneamino)-ethenolate | HCID 86600794 | 60% |
Reaction Steps
To a stirred suspension of 3.222 g (36 mmol, 1.05 eq) of potassium ethoxide in 30 mL diethyl ether and 5 mL EtOH at 0° C., a solution of 3.849 g (52 mmol, 1.5 eq) ethyl formate and 6 g (35 mmol) (1-ethoxy-ethylideneamino)-acetic acid ethyl ester in 30 mL diethyl ether and 5 mL EtOH is then slowly added. The reaction mixture is stirred for one hour at 0° C. After addition of 40 mL diethyl ether, the reaction mixture was stirred at RT overnight. The reaction mixture was filtered and the obtained solid was washed with diethyl ether and dried under vaccum to yielded 5 g (60%) of potassium 2-ethoxycarbonyl-2-(1-ethoxy-ethylideneamino)-ethenolate as an orange solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906546B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-7604398ec82245c4bb68a8a1f10f6e79 |
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| Source note | uspto-grants-2011_03 |
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