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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928376Generated: October 30, 2026

HCID 58081337, compound → HCID 58081240, compound

https://huagongshe.com/reaction/928376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58081337HCID 58081337—
SolventEthanol tetrahydrofuran waterHCID 18504229—
ProductHCID 58081240HCID 58081240—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of crude ethyl 1-(4-((1H-pyrazol-1-yl)methyl)-3-methoxybenzyl)-1H-pyrazole-4-carboxylate (998 mg, 29%, 0.85 mmol) in THF:EtOH:H2O 2:1:1 (15 ml), LiOH Monohydrate (107 mg, 2.55 mmol) was added and stirred for 12 h at 50° C. The reaction mixture was concentrated under reduced pressure. The remaining solid was taken up in ethyl acetate and extracted with water. The aqueous phase was acidified by adding aqueous HCl and extracted with ethy acetate. The organic extract was dried over Na2SO4, filtered and concentrated under reduced pressure to afford crude 1-(4-((1H-pyrazol-1-yl)methyl)-3-methoxybenzyl)-1H-pyrazole-4-carboxylic acid. MS [M+H]+=313.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290485B2
Source datasetuspto-grants-2016_03
ORD IDord-08e5c856262b47da98bdc189d439abcd
Source noteuspto-grants-2016_03