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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330056Generated: October 25, 2026

1,3,5-Tri-tert-butylbenzene → 1,3,5-tri(tertbutyl)benzene Yttrium

https://huagongshe.com/reaction/330056

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-Tri-tert-butylbenzeneHCID 15089—
ReactantYttriumHCID 23993—
Product1,3,5-tri(tertbutyl)benzene YttriumHCID 86743687—

Reaction Steps

Vapourised yttrium [ca 0.9 g (10 mmol)] was cocondensed with 25 g (100 mmol) of 1,3,5-tri(tertbutyl) benzene at -196° C. over a period of 2 hours. The cocondensate was allowed to warm to room temperature under argon and the solid products extracted from the apparatus with n-hexane (ca 750 cm3). The resultant deep purple solution was filtered through a bed of Celite on a frit and the solvent removed under reduced pressure. Excess of the 1,3,5-tri(tertbutyl)benzene was then removed by the sublimation at 60° C./10-4 mbar and the residue extracted with n-pentane (ca 150 cm3). The resulting solution was again filtered through Celite. Concentration of the resultant solution under reduced pressure and cooling to -30° C. afforded deep purple crystals of the complex. The crystals were collected, washed with n-pentane at -80° C. (2×10 cm3) and dried in vacuo. Yield ca 2.4 g (40% based on yttrium).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894446
Source datasetuspto-grants-1990_01
ORD IDord-0b241699311f44d8a2914b29b90705cc
Source noteuspto-grants-1990_01