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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419155Generated: November 1, 2026

Carbon Dioxide → HCID 20314771, compound

https://huagongshe.com/reaction/2419155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantEthanolHCID 702—
Reactant3-(Methylsulfanyl)-1,2,4-triazineHCID 321839—
ReactantSodiumHCID 5360545—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 20314771HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105434
Source datasetuspto-grants-1978_08
ORD IDord-49a9378e0e4d491689ae0f73eae83507
Source noteuspto-grants-1978_08