Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | HCID 21438967 | HCID 21438967 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21438996 | HCID 21438996 | 37.8% |
Reaction Steps
A suspension of 40 g of ethyl N-carbethoxy-dithiocarbamate, 14 g of potassium methylate, 15 g of chloroacetonitrile and 1 g of potassium iodide in 250 ml of methanol was stirred for 3 hours at room temperature under an inert atmosphere and then 14 g of potassium methylate were added. The reaction mixture was refluxed for one hour and water was then added thereto. The aqueous phase was washed with ethyl acetate and then acidified with concentrated hydrochloric acid. The aqueous phase was extracted with ethyl acetate and the extracts were dried, filtered and evaporated to dryness. The residue was empasted with isopropyl ether and then filtered to obtain 14 g of 2-ethylthio-4-hydroxy-5-cyano-thiazole in the form of cream crystals melting at 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04020076 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-90e179088b2542f0a9c64c08e0689529 |
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| Source note | uspto-grants-1977_04 |
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