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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735983Generated: October 26, 2026

Water → (-)-2-(4-(4-Octyloxy-5,5,5-trifluoro-1-pentyl)phenyl)-5-decyloxypyrimidine

https://huagongshe.com/reaction/1735983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium hydrideHCID 82127—
Reactantn-Octyl p-ToluenesulfonateHCID 599296—
Reactant(-)-2-(4-(4-Hydroxy-5,5,5-trifluoro-1-pentyl)phenyl)-5-decyloxypyrimidineHCID 19694914—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(-)-2-(4-(4-Octyloxy-5,5,5-trifluoro-1-pentyl)phenyl)-5-decyloxypyrimidineHCID 1943504356.7%

Reaction Steps

1.1 g (2.5 mmol) of (-)-2-(4-(4-hydroxy-5,5,5-trifluoro-1-pentyl)phenyl)-5-decyloxypyrimidine was dissolved in 10 ml of tetrahydrofuran. This solution was added with 0.12 g (3 mmol) of potassium hydride, stirred at 10°-20° C. for 20 minutes, further added with 0.85 g (3 mmol) of octyl p-toluenesulfonate and reacted at 20°-30° C. for 2 hours. The reaction mixture was poured into 100 ml of water and 100 ml of toluene, and the toluene layer was washed with water and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using toluene/ethyl acetate as eluent to obtain 0.80 g of (-)-2-(4-(4-octyloxy-5,5,5-trifluoro-1-pentyl)phenyl)-5-decyloxypyrimidine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539115
Source datasetuspto-grants-1996_07
ORD IDord-1789afb5355746d8aebc00d8001c9cc7
Source noteuspto-grants-1996_07