HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582980Generated: October 30, 2026
5-Octyl-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine → 5-Octyloxy-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine
https://huagongshe.com/reaction/582980
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Octyl-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine | HCID 21225304 | — |
| Reactant | Phenol, 4-[5-(octyloxy)-2-pyrimidinyl]- | HCID 135708811 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Octyloxy-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine | HCID 21225286 | — |
Reaction Steps
The title compound was prepared essentially as in Example 1 by combining 3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)-1-chloropropane (5.2 g, 10.9 mmol, Example 24) with 5-octyloxy-2-(4-hydroxyphenyl)pyrimidine (3 g, 10.0 mmol) in dimethylformamide and stirring at 120° C. overnight. The resulting product was further purified by Kugelrohr distillation (b.p. 195-210° C. at 0.3 torr), followed by recrystallization from ethanol and additional distillation (yield of 3.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05928562 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-93dfcce0311747ac8d58e6cda8fcd803 |
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| Source note | uspto-grants-1999_07 |
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