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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177935Generated: October 25, 2026

Hydrochloric Acid → 4-(4-Methylpiperazin-1-yl)benzoic acid

https://huagongshe.com/reaction/1177935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 4-(4-methylpiperazin-1-yl)benzoateHCID 1472668—
SolventOxolane--water (1/1)HCID 21881883—
Product4-(4-Methylpiperazin-1-yl)benzoic acidHCID 73653285.13%

Reaction Steps

LiOH (67 mg, 1.6 mmol) was added to a stirred solution 4-(4-methyl-piperazin-1-yl)-benzoic acid methyl ester (124 mg, 0.73 mmol) in THF:H2O (1:1, 4 mL), and the resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure to get the residue. Cold water was then added and acidified it with 10% aqueous HCl and concentrated under reduced pressure to afford 116 mg (85.13% yield) of 4-(4-methyl-piperazin-1-yl)-benzoic acid. 1H NMR (DMSO-D2O): δ 7.8 (d, 2H), 7.0 (d, 2H), 3.4 (s, 4H), 2.8 (s, 4H), 2.4 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-e3ae7b1d8a90423cacf494b73e07d6df
Source noteuspto-grants-2010_11