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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053993Generated: October 30, 2026

Hydrochloric Acid → 1-(2-Benzyloxy-5-bromo-benzyl)-5-Trifluoromethyl-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1053993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Pyrazole-3-carboxylic acid, 5-(trifluoromethyl)-, ethyl esterHCID 2726919—
Reactant1-(Benzyloxy)-4-bromo-2-(bromomethyl)benzeneHCID 11783220—
SolventDimethylformamideHCID 6228—
Product1-(2-Benzyloxy-5-bromo-benzyl)-5-Trifluoromethyl-1H-pyrazole-3-carboxylic acid ethyl esterHCID 8668569467.7%

Reaction Steps

To a solution of 5-trifluoromethyl-1H-pyrazole-3-carboxylic acid ethyl ester (0.114 g, 0.55 mmol) and 1-benzyloxy-4-bromo-2-bromomethyl-benzene (0.196 g, 0.55 mmol) in DMF (2 ml) cooled at RT under N2 atmosphere was added K2CO3 (0.19 g, 1.375 mmol) The mixture was stirred at RT overnight, then acidified with HCl (2M, aq.) and extracted with EtOAc. The organic layer was separated, washed with brine, dried (MgSO4) and evaporated to dryness. The residue was purified by MPLC (10 g SiO2 cartridge, eluent 90% iso-hexane-10% EtOAc) yielding 0.18 g of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394284B2
Source datasetuspto-grants-2016_07
ORD IDord-710dcf2459bf4c22b1131f8e708285ec
Source noteuspto-grants-2016_07