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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1763181Erstellt: 26. Oktober 2026

Azobenzene → 2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxide

https://huagongshe.com/reaction/1763181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobenzeneHCID 2272—
EduktDichloneHCID 8342—
EduktFluorenoneHCID 10241—
EduktSodium HydroxideHCID 14798—
EduktPhenol, 2-[2-(4-chloro-2-nitrophenyl)diazenyl]-6-(1,1-dimethylethyl)-4-methyl-HCID 89771—
Edukt(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxideHCID 14149470—

Reaktionsschritte

97% sodium hydroxide 8.2 g was added and dissolved in a mixture of methanol 60 ml and water 20 ml. 2-nitro-4-chloro-2'-hydroxy-3'-t-butyl-5'-methylazobenzene 11.6 g was then added to the resultant solution at 50° to 60° C. over 30 minutes while stirring, and thereafter 2,3-dichloro-1,4-naphthoquinone 0.3 g and 9-fluorenone 0.4 g were added to the solution. Glucose 4 g was then added to the resultant mixture at 40° to 50° C. over two hours, and the mixture was stirred for one hour at the same temperature. As this result, almost all of the azobenzene disappeared to produce 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole-N-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04835284
Quelldatensatzuspto-grants-1989_05
ORD IDord-ac06adbe2c7f48489253bb102ad6ed39
Quellennotizuspto-grants-1989_05