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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990205Generated: October 25, 2026

Hydrochloric Acid → 5-n-Butylthio-2-(2-hydroxy-3-alpha-cumyl-5-tert-octylphenyl)-2H-benzotriazole

https://huagongshe.com/reaction/990205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButanethiolHCID 8012—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantPotassium HydroxideHCID 14797—
Reactant5-chloro-2-(2-hydroxy-3-alpha-cumyl-5-tertoctylphenyl)-2H-benzotriazoleHCID 21885009—
Product5-n-Butylthio-2-(2-hydroxy-3-alpha-cumyl-5-tert-octylphenyl)-2H-benzotriazoleHCID 1867283883%

Reaction Steps

5-Chloro-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl)-2H-benzotriazole (38.1 g, 0.08 mol), n-butyl mercaptan (9 g, 0.10 mol), potassium hydroxide (10.1 g, 0.18 mol) and N-methylpyrrolidone (99 g, 1.0 mol) are charged to a reactor and heated to 170°0C. The reaction mass is held at 170° C. with vigorous stirring for five hours. The reaction is judged as complete using thin layer chromatography. The temperature is reduced to 5° C. and 100 mL of aqueous 2N hydrochloric acid are then added to the reactor. The liquid is decanted and the solids are dissolved in ethyl acetate. The organic layer is washed with aqueous 2N hydrochloric acid followed by water. The ethyl acetate is stripped off and the product is crystallized from ethanol and toluene. The title compound is obtained as a yellow crystalline product in 83% yield. The structure is verified by 1Hnmr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458872B1
Source datasetuspto-grants-2002_10
ORD IDord-c2ad1ae793564f0e9ff46f3c868c145f
Source noteuspto-grants-2002_10