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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233309Generated: October 31, 2026

Tricyclohexylphosphine → HCID 59295455, compound

https://huagongshe.com/reaction/2233309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Bromo-4-(bromomethyl)benzonitrileHCID 53425521—
ReactantHCID 59295410HCID 59295410—
ReactantHCID 59295451HCID 59295451—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 59295455HCID 59295455—

Reaction Conditions

Temperature100 °C

Reaction Steps

309 mg 2-Bromo-4-{2,2,2-trifluoro-1-[4-methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-ethoxymethyl}-benzonitrile (derived from 2,2,2-Trifluoro-1-[4-methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-ethanol and 2-Bromo-4-bromomethyl-benzonitrile according to the method described in example 30), 32 mg tricyclohexylphosphine, 148 mg cyclopropylboronic acid and 470 mg K3PO4 mono hydrate were dissolved in a mixture of 4 ml toluene and 0.4 ml water. The reaction mixture was purged with argon, then 130 mg palladium (II) acetate were added. The reaction mixture was stirred at 100° C. for three hours. The cooled reaction mixture was diluted by addition of 100 ml ethyl acetate and filtered through a celite pad. The filtrate was washed twice with 25 ml water, then dried over MgSO4. The solvent was removed in vacuo. The resulting residue was purified by reversed phase HPLC to obtain 185 mg 2-Cyclopropyl-4-{2,2,2-trifluoro-1-[4-methyl-2-(6-trifluoromethyl-pyridin-3-yl)-thiazol-5-yl]-ethoxymethyl}-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709481B2
Source datasetuspto-grants-2010_05
ORD IDord-ba606e0effa149cf89184e9540bd50f1
Source noteuspto-grants-2010_05