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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351236Generated: October 30, 2026

Thioanisole → 4-[3-Chloro-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]phenol

https://huagongshe.com/reaction/351236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
Reactant5-[4-(benzyloxy)phenyl]-3-chloro-1-(4-methoxyphenyl)-1H-pyrazoleHCID 21090901—
Product4-[3-Chloro-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]phenolHCID 13573737421.3%

Reaction Steps

A solution of 4-[3-chloro-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]phenyl benzyl ether (2.79 g) and thioanisole (3.56 g) intrifluoroacetic acid (25 ml) was stirred at ambient temperature overnight. The mixture was concentrated in vacuo. The residue was recrystallized from AcOEt (15 ml) and n-hexane (12 ml) to give 1st crop of FR282117 (1.48 g). The mother liqour was washed with H2O, saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted with AcOEt/n-hexane=30%. The pure fractions were collected and concentrated in vacuo. The residual crystals were collected and washed with IPE to give 2nd crop of 4-[3-chloro-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]phenol(457.2 mg) white powder

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183306B2
Source datasetuspto-grants-2007_02
ORD IDord-a070a00f587e49959f29e4a8a3b456be
Source noteuspto-grants-2007_02