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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623694Generated: October 31, 2026

Hydrochloric Acid → 5-[(4-Methyl-1-piperazinyl)sulfonyl]-2-[(phenylmethyl)oxy]benzoic acid

https://huagongshe.com/reaction/1623694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 5-[(4-methyl-1-piperazinyl)sulfonyl]-2-[(phenylmethyl)oxy]benzoateHCID 67107392—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-[(4-Methyl-1-piperazinyl)sulfonyl]-2-[(phenylmethyl)oxy]benzoic acidHCID 67107215—

Reaction Conditions

Temperature50 °C

Reaction Steps

LiOH (15.39 mg, 0.64 mmol) was added to a stirred solution of methyl 5-[(4-methyl-1-piperazinyl) sulfonyl]-2-[(phenylmethyl)oxy]benzoate (may be prepared as described in Description 71; 260 mg, 0.64 mmol) in a mixture of tetrahydrofuran and water (3:1, 40 ml). The mixture was heated at 50° C. for 6 h and then diluted with ethyl acetate (50 nil). 10% Aqueous HCl was added to the mixture to adjust pH to 2. The organic phase was isolated, washed with brine, dried over MgSO4, and concentrated to yield the title compound as a white solid. 120 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-9f4cd88d4e0045d495e1a61ab6a4e668
Source noteuspto-grants-2014_07