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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250492Generated: November 2, 2026

3-(Trifluoromethyl)phenol → HCID 15906604, compound

https://huagongshe.com/reaction/1250492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18326222HCID 18326222—
CatalystCupric ChlorideHCID 24014—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 15906604HCID 15906604—

Reaction Conditions

Temperature120 °C

Reaction Steps

1.04 g (0.0029×2.2 mol) of 3-(trifluoromethyl) phenol was dissolved in about 10 ml of DMF. The obtained solution was further mixed with 0.24 g (ca. 60% in mineral oil; 0.0029×2.0 mol) of NaH and then with 0.94 g (0.0029 mol) of N-benzyl-6-bromo-4-methoxy-2-pyridine carboxamide. After adding 0.15 g (0.0029×0.5 mol) of copper chloride (I), the solution was stirred at about 120° C. for about 5 hours, and then allowed to stand for cooling to room temperature. After the reaction solution was distributed in ethyl acetate-saturated sodium bicarbonate water, the organic phase of the solution was washed with saturated brine and dried with anhydrous sodium sulfate, followed by concentration thereof. Thereafter, the concentrated solution was purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339045B1
Source datasetuspto-grants-2002_01
ORD IDord-96976284f202477cbcea5228ce346bed
Source noteuspto-grants-2002_01