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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623666Generated: October 26, 2026

Hydrochloric Acid → 2-(Benzyloxy)-5-(piperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/1623666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantBenzyl 2-(benzyloxy)-5-(piperidin-1-yl)benzoateHCID 66990101—
SolventEthyl AcetateHCID 8857—
SolventOxolane--water (1/1)HCID 21881883—
Product2-(Benzyloxy)-5-(piperidin-1-yl)benzoic acidHCID 66991063—

Reaction Steps

LiOH (1.25 mL, 3.74 mmol) was added to a stirred solution of phenylmethyl 2-[(phenylmethyl)oxy]-5-(1-piperidinyl)benzoate (may be prepared as described in Description 41; 150 mg, 0.37 mmol) in a mixture of THF:water (3:1, 10 ml). The mixture was heated to reflux for 12 h and then diluted with ethyl acetate (50 ml). 10% aqueous HCl was added to the mixture to adjust the pH to 2. The organic phase was isolated, washed with brine, dried over magnesium sulphate, and concentrated to give a yellow oil. The crude product was purified using Comflash to yield the title compound. 80 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-2761f3d84155469c83b5acc5ae5a4655
Source noteuspto-grants-2014_07