Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-(Methylsulfanyl)-1,2,4-triazine | HCID 321839 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20314771 | HCID 20314771 | — |
Reaction Steps
Sodium (30.8g - 1.34g.atm) is reacted with 6 pints of absolute ethyl alcohol below 43° C. 3- Methylthio-1,2,4-triazine (159 g. - 1.25 m) is added, and the black mixture stirred under nitrogen at 40° to 44° C. for 34 minutes. The heating bath is replaced by ice water and carbon dioxide gas bubbled in, giving a red-orange mixture at pH 9 within 23/4 hours. Water (1.25 m) is added and carbon dioxide addition continued for 35 minutes without visible or pH change. Air is introduced for another half hour, giving a brown mixture. One liter of benzene is added and the contents filtered with suction at 19° C. The solids are slurried in a liter of water and extracted with CHCl3 several times. The combined filtrate and extracts are vacuum distilled, giving 3-ethoxy-1,2,4-triazine, b.p. 113°-115° C. at 16 mm. The pot residue is recrystallized from methanol to give 16 g. of golden brown platelets, m.p. 95°-99° C. Recrystallizing again from methanol, and finally from ethyl alcohol, yields 7.7 g. of 3,3'-diethoxy-5,5'-bis-1,2,4-triazinyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04105434 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-49a9378e0e4d491689ae0f73eae83507 |
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| Source note | uspto-grants-1978_08 |
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