HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440189Generated: October 26, 2026
p-Toluenesulfonic acid → 5-Phenylthio-2-[2-hydroxy-3-tert-butyl-5-(beta-octyloxycarbonylethyl)phenyl]-2H-benzotriazole
https://huagongshe.com/reaction/440189
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 3-(5-phenylthio-2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamic acid | HCID 21218128 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Phenylthio-2-[2-hydroxy-3-tert-butyl-5-(beta-octyloxycarbonylethyl)phenyl]-2H-benzotriazole | HCID 21218132 | 96% |
Reaction Steps
Likewise, to a 250 mL round-bottomed flask equipped with a magnetic stirrer, nitrogen inlet, condenser, and a Dean-Stark trap are charged 4.3 g (0.0096 mol) of 3-(5-phenylthio-2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamic acid, 3.4 g (0.026 mol) of Exxel 8, an isomeric mixture of octanols available from Exxon Chemicals, 70 mg of p-toluenesulfonic acid, and 20 mL of xylene. The mixture is refluxed 3.5 hours, is cooled to room temperature, and a portion of ethyl acetate is added. The solution is washed once with water, twice with saturated sodium bicarbonate solution, and once with brine. After drying over anhydrous magnesium sulfate, the solvent is removed under reduced pressure to afford 5.17 g (96% yield) of the title compound as a viscous yellow oil. Analysis by nmr (CDCl3) is consistent with the structure of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516914 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-831a9699a74c4bbba7d4b1ab755e233c |
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| Source note | uspto-grants-1996_05 |
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