Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20536293 | HCID 20536293 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20536285 | HCID 20536285 | — |
Reaction Steps
10.0 g (0.014 mol) of 1-chloro-3,5-di-[3-(3,5-di-tert.butyl-4-hydroxyphenyl)-2,2-dimethylpropylamino]-s-triazine (the product of Example 64) and 2.91 g (0.044 mol) of dodecylmercaptan are initially introduced into 50 ml of acetone and 0.58 g (0.0144 mol) of sodium hydroxide, dissolved in 1 ml of water, is added at room temperature. The mixture is then heated to the point of reflux and is stirred at this temperature for 5 hours. It is then cooled, insoluble matter is filtered off and the filtrate is concentrated completely. The residue is purified through a silica gel column using toluene:methanol (98:2) as the migrating agent. The 1-dodecylmercapto-3,5-di-[3-(3,5-di-tert.butyl-4-hydroxyphenyl)-2,2-dimethylpropylamino]-s-triazine obtained in this way is produced as a yellowish resin. (Stabiliser No. 68).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04333868 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-322be3ebb30f45aba525c86cb6d491aa |
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| Source note | uspto-grants-1982_06 |
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