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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971910Generated: October 30, 2026

1-Octanethiol → HCID 21312513, compound

https://huagongshe.com/reaction/971910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OctanethiolHCID 8144—
ReactantSodiumHCID 5360545—
ReactantHCID 21312534HCID 21312534—
SolventMethanolHCID 887—
ProductHCID 21312513HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04161592
Source datasetuspto-grants-1979_07
ORD IDord-073cb6b6ad3f4d3d8b36b2ccb91e49c3
Source noteuspto-grants-1979_07