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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526033Generated: October 26, 2026

Hydrochloric Acid → 2-Nitro-4-piperidin-1-ylmethyl-benzoic acid hydrochloride

https://huagongshe.com/reaction/1526033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Nitro-4-(piperidine-1-carbonyl)-benzoic acid tert-butyl esterHCID 68672086—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
Product2-Nitro-4-piperidin-1-ylmethyl-benzoic acid hydrochlorideHCID 68671001—

Reaction Steps

2-Nitro-4-(piperidine-1-carbonyl)-benzoic acid tert-butyl ester (1.87 mmol) was dissolved in dry THF and added drop-wise to 3.7 mL of borane tetrahydrofuran complex 1.0 M solution, at room temperature, under nitrogen, with stirring. The reaction was then refluxed for six hours, cooled to room temperature and treated carefully with 2N HCl (10 mL) After stirring for 15 minutes, solid K2CO3 was added in portions (1.75 g). The mixture was extracted with EtOAc (3×25 mL). The combined organic layers were dried over sodium sulphate and evaporated leaving an oil that by HPLC-MS analysis resulted a 4:6 mixture of the tertiary amine and the corresponding borane complex. The mixture was dissolved in DCM (1 mL) and treated with 4N HCl in dioxane (7 mL). After 4 days at room temperature, an off white was formed which was filtered, washed with dioxane (5 mL) and dried at 50° C. under vacuum. 0.40 g of title compound were obtained in 70% overall yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085558B2
Source datasetuspto-grants-2015_07
ORD IDord-01a94e90742d408e9e915a75b1d52719
Source noteuspto-grants-2015_07