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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296943Generated: October 30, 2026

Boron Trichloride → HCID 178488687, compound

https://huagongshe.com/reaction/1296943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58913529HCID 58913529—
SolventDichloromethaneHCID 6344—
ProductHCID 178488687HCID 178488687—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-(2-Benzyloxy-5-chloro-4-fluoro-phenyl)-4-(4-methoxy-phenyl)-3-methyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazole (1 eq) was taken up in anhydrous dichloromethane and the solution was cooled under nitrogen to 0° C. 1M boron trichloride in dichloromethane (6 eq) was added dropwise and the solution was allowed to stir for 1 hour. The reaction mixture was added dropwise to sat. NaHCO3 (aq) and the resulting solution was extracted into dichloromethane. The organic phases were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by preparative LC/MS, to give 4-chloro-5-fluoro-2-[4-(4-methoxy-phenyl)-5-methyl-2H-pyrazol-3-yl]-phenol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247734B2
Source datasetuspto-grants-2007_07
ORD IDord-ef8f3ee3afe949c7932d34e0359ce409
Source noteuspto-grants-2007_07