Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | 2-(1-Ethoxypropylidene)malononitrile | HCID 231470 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15565693 | HCID 15565693 | 85.3% |
Reaction Steps
Ethanol, (11.0 L), 2-(1-ethoxy-propylidene)-malononitrile, (2.003 kg, 13.34 moles, 1.0 eq), ethyl-2-mercaptoacetate (1.652 kg, 13.34 moles, 1.0 eq.), and potassium acetate (1.983 kg, 20.0 moles, 1.5 eq.) are charged to a 22L 3-neck reaction flask equipped with an addition funnel, thermocouple, overhead stirrer, and condenser. The reaction mixture becomes dark red and exotherms to 72° C. The mixture is stirred for 1.25 hours while cooling to 60° C. Deionized water (2.6 L), is added to the reaction mixture over 30 minutes while cooling to 53° C. The reaction mixture is then cooled to 10° C. over 3.5 hours. The resulting suspension is filtered to recover the precipitate, and the filter cake is rinsed with a chilled mixture of 1.1 L ethanol and 3.9 L water. The filter cake is vacuum dried at room temperature, affording the title compound (2.552 kg) in 85.3% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642361B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-a0d7f5c3c39c4f7ab199f4eb81e8fa1a |
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| Source note | uspto-grants-2010_01 |
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