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HRID 278511Erstellt: 25. Oktober 2026

Pentamethylbenzene → 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one

https://huagongshe.com/reaction/278511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentamethylbenzeneHCID 12784—
EduktTin tetrachlorideHCID 24287—
Edukt5,7-Di-tert-butyl-3-hydroxy-2-benzofuranoneHCID 6850821—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelWaterHCID 962—
Produkt5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-oneHCID 1091619689,3%

Reaktionsschritte

11.5 g (77.5 mmol) of pentamethylbenzene and 10 ml (85.0 mmol) of tin tetrachloride are added to a solution of 19.7 g (75.0 mmol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example la) in 50 ml of 1,2-dichloroethane and the reaction mixture is refluxed for 1 hour. The reaction mixture is diluted with water and extracted three times with toluene. The organic phases are combined, washed with water, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. Crystallisation of the residue from ethanol yields 26.3 g (89%) of 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one, m.p. 185-190° C. (compound (111), Table 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06359148B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-d2f17aff12324320af64444ee601ac30
Quellennotizuspto-grants-2002_03