HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octanethiol → HCID 21312513, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octanethiol | HCID 8144 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 21312534 | HCID 21312534 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21312513 | HCID 21312513 | — |
Reaction Steps
1.15 g of sodium were dissolved in 150 ml of methanol and 7.3 g of n-octylmercaptan were added. A solution of 10.8 g of 2-(3-tert.-butyl-5-methyl-4-hydroxyanilino)-4-[(2,2,6,6-tetramethyl-piperidin-4-yl)-amino]-6-chloro-1,3,5-triazine in 200 ml of methanol was added to the resulting sodium n-octylmercaptide, whilst stirring. The reaction mixture was kept under reflux for 16 hours and then poured into 400 ml of ice water, a slightly brownish precipitate, which was filtered off, being formed. Recrystallization from ethyl acetate/hexane gives 13.9 g of almost colourless 2-(3-tert.-butyl-5-methyl-4-hydroxyanilino)-4-[(2,2,6,6-tetramethyl-piperidin-4-yl)-amino]-6-(n-octylthio)-1,3,5-triazine having a melting point of 133° C. (stabiliser 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04161592 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-073cb6b6ad3f4d3d8b36b2ccb91e49c3 |
| Source note | uspto-grants-1979_07 |