HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990203Generated: October 26, 2026
Hydrochloric Acid → 5-n-Butylthio-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotnazole
https://huagongshe.com/reaction/990203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol | HCID 77470 | — |
| Product | 5-n-Butylthio-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotnazole | HCID 18672839 | — |
Reaction Steps
5-Chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)2H-benzotriazole (21.2 g, 0.06 mol), n-butyl mercaptan (7.2 g, 0.08 mol), potassium hydroxide (6.7.1 g, 0.12 mol) and N-methylpyrrolidone (50 g, 0.5 mol) are charged to a reactor and heated to 150° C. The reaction mass is held at 150° C. for 4.5 hours at which time it then cooled to ambient temperature. A mixture of 15 g of concentrated hydrochloric acid aand 70 g of ice are then added to the reactor. The solids are filtered off and washed with water. Thirty gram of crude, wet, yellow crystals are obtained as the title compound. This product can be used “as is” in procedure of Example 33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458872B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3474b9ee14db4f6a94ff41124b3e11d1 |
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| Source note | uspto-grants-2002_10 |
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