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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76116Generated: October 25, 2026

Benzoyl chloride → HCID 44219523, compound

https://huagongshe.com/reaction/76116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178459030HCID 178459030—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 44219523HCID 4421952322.7%

Reaction Steps

To a solution of 2-(1H-indazol-3-ylmethoxy)-2-methylpropanoic acid (6 g; 0.026 mol) in acetone (50 ml) stirred at room temperature was added K2CO3 (6.8 g; 0.049 mol) and then, slowly, a solution of benzoyl chloride (5 ml; 0.043 mol) in acetone (30 ml). The mixture was stirred at room temperature for 24 hours and then poured into water (1 L). The solution was then brought to basic pH with 5N NaOH and washed with diethyl ether (3×150 ml). The alkaline phase was then acidified with concentrated HCl and extracted with diethyl ether (3×300 ml). The combined organic phases were concentrated under reduced pressure and the crude residue obtained was purified by crystallization from a 1/1 hexane/ethyl acetate mixture. 2 g of 2-[(1-benzoyl-1H-indazol-3-yl)methoxy]-2-methylpropanoic acid were obtained, m.p.=132-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835481B2
Source datasetuspto-grants-2014_09
ORD IDord-66d08c1482514ff997c4bd7988b314be
Source noteuspto-grants-2014_09