Dibutyltin oxide → 2,2'-{(Dibutylstannylene)bis[oxy-(5-tert-octyl-2,l-phenylene)]}bis-(2H-benzotriazole)

HRID 433652

Reaktionsgleichung

Reaktionsgleichung von HRID 433652
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:10])[CH3:9])=[CH:4][C:3]=1[N:16]1[N:20]=[C:19]2[CH:21]=[CH:22][CH:23]=[CH:24][C:18]2=[N:17]1.[CH2:25]([Sn:29](=[O:34])[CH2:30][CH2:31][CH2:32][CH3:33])[CH2:26][CH2:27][CH3:28]>C1(C)C=CC=CC=1>[CH2:25]([Sn:29]([CH2:30][CH2:31][CH2:32][CH3:33])([O:34][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH2:11][C:12]([CH3:13])([CH3:14])[CH3:15])([CH3:9])[CH3:10])=[CH:4][C:3]=1[N:16]1[N:17]=[C:18]2[CH:24]=[CH:23][CH:22]=[CH:21][C:19]2=[N:20]1)[O:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH2:11][C:12]([CH3:13])([CH3:14])[CH3:15])([CH3:9])[CH3:10])=[CH:4][C:3]=1[N:16]1[N:20]=[C:19]2[CH:21]=[CH:22][CH:23]=[CH:24][C:18]2=[N:17]1)[CH2:26][CH2:27][CH3:28]

Komponenten

4

Edukt 2

HCID 61221Dibutyltin oxideHCID 62485Octrizole

Produkt 1

HCID 700158602,2'-{(Dibutylstannylene)bis[oxy-(5-tert-octyl-2,l-phenylene)]}bis-(2H-benzotriazole)Ausbeute 43,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

2-(2-Hydroxy-5-tert-octylphenyl)-2H-benzotriazole (64.6 g, 0.2 mol, TINUVIN® 329, CIBA), dibutyltin oxide (24.89 g, 0.1 mol) and toluene are charged to a laboratory reactor and the contents are heated to reflux and refluxed for seven hours. About half of the amount of toluene is removed by distillation. The reaction mass is cooled to 0-5° C. after the addition of 200 g of hexane. Any unreacted TINUVIN® 329 and dibutyltin oxide are removed by filtration. The solvent is then removed by distillation to yield the title compound (38 g, 43.3% yield) as a yellow resin whose structure is consistent with 1Hnmr analysis.

Aufarbeitung

  1. temperaturethe contents are heated
  2. temperatureto reflux
  3. temperaturerefluxed for seven hours
  4. customAbout half of the amount of toluene is removed by distillation
  5. additionafter the addition of 200 g of hexane
  6. customAny unreacted TINUVIN® 329 and dibutyltin oxide are removed by filtration
  7. customThe solvent is then removed by distillation

Quellen und Nachweise

ORD-Eintrag
ord-4819dd734c184c8e900ec89be064cb1a
Quelldatensatz
uspto-grants-2003_12
Patentnummer
US06667403B2

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