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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623691Generated: November 2, 2026

Hydrochloric Acid → 2-[(Phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoic acid

https://huagongshe.com/reaction/1623691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 2-[(phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoateHCID 67107209—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-[(Phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoic acidHCID 67107473—

Reaction Conditions

Temperature50 °C

Reaction Steps

LiOH (20.29 mg, 0.847 mmol) was added to a stirred solution of methyl 2-[(phenylmethyl)oxy]-5-(1-piperidinylsulfonyl)benzoate (may be prepared as described in Description 68; 330 mg, 0.85 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 ml). 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. 220 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-6863559b5fd24c1a933c02eaf3c10166
Source noteuspto-grants-2014_07