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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122168Generated: November 3, 2026

Cesium carbonate → HCID 88057141, compound

https://huagongshe.com/reaction/2122168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantHCID 87792257HCID 87792257—
SolventAcetonitrileHCID 6342—
ProductHCID 88057141HCID 88057141—

Reaction Conditions

Temperature50 °C

Reaction Steps

3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl](1,1,1-trifluoro-2-hydroxypropyl)-amino]phenol (100 mg, 0.23 mmol) and bromomethylcyclohexane (42 μL, 0.30 mmol) were dissolved in 2 mL of acetonitrile. Cesium carbonate (144 mg, 0.44 mmol) was added, and the stirred solution was warmed to 50° C. for 48 hours, at which time HPLC analysis indicated that no phenolic starting material remained. The reaction was quenched with water and filtered through pre-wetted celite eluting with ethyl acetate. The solvent was evaporated and the residue was purified by reverse phase HPLC eluting with 10% to 90% acetonitrile in water to afford 55 mg (35%) of the desired ether product as a brown oil, which was greater than 99% pure by reverse phase HPLC analysis. HRMS calcd. for C25H29F7NO3: 524.2036 [M+H]+, found: 524.2028. 1H NMR (CDCl3) δ0.9-1.4 (m, 5H), 1.7-1.9 (m, 6H), 3.6 (m, 3H), 3.9 (dd, 1H), 4.3 (m, 1H), 4.7 (m, 2H), 5.1 (s, 1H), 5.9 (tt, 1H), 6.5 (m, 3H), 7.0-7.4 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696472B2
Source datasetuspto-grants-2004_02
ORD IDord-c897c3412d754605b23d8c48a60898be
Source noteuspto-grants-2004_02