2-(4-Hydroxyphenyl)-5-octylpyrimidine → HCID 21225284, compound

Participants

Reaction Steps

The title compound was prepared essentially as in Example 1 by combining 5-octyl-2-(4-hydroxyphenyl)pyrimidine (8.0 g, 28.13 mmol) and 6-(2-(nonafluorobutoxy)-2,2-difluoroethoxy)-1-bromohexane (14.15 g, 29.54 mmol; prepared by combining 1,6-dibromohexane with 2-(nonafluorobutoxy)-2,2-difluoroethanol). After refluxing overnight, the resulting crude product was isolated by filtration and further purified by recrystallization from ethanol, followed by Kugelrohr distillation (b.p. 200° C. at 0.25 torr).

Provenance & Evidence