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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279391Generated: November 2, 2026

Hydrochloric Acid → HCID 178497572, compound

https://huagongshe.com/reaction/1279391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium sulfide nonahydrateHCID 73972—
Reactant2,3-Diaminobenzoic acid methyl esterHCID 571825—
Reactant1-Acetylpiperidine-4-carbaldehydeHCID 18428037—
CatalystCupric acetateHCID 8895—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178497572HCID 17849757275%

Reaction Steps

3.3 g (19.9 mmol) of methyl 2,3-diaminobenzoate were dissolved in 100 ml of methanol, and a solution of 4.0 g (25.8 mmol) of N-acetylpiperidine-4-carbaldehyde in 100 ml of methanol was added dropwise at room temperature. The whole was stirred for about 10 minutes at room temperature. Thereafter, 5.2 g (25.8 mmol) of copper(II) acetate, which was dissolved in 100 ml of water, were added dropwise and the whole was refluxed for 30 minutes. After cooling, 25 ml of concentrated hydrochloricacid were added carefully and the whole was again refluxed. 7.15 g (29.8 mmol) of sodium sulfide nonahydrate, dissolved in 100 ml of water, were then added dropwise and the whole was boiled for a further 10 minutes. After cooling, the reaction solution was evaporated down under reduced pressure. The residue obtained was dispersed in water and filtered. The filtrate was rendered alkaline with aqueous sodium bicarbonate solution and was extracted several times with ethyl acetate. The combined organic phases were washed with water, dried and evaporated down under reduced pressure. 4.5 g of the product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448271B1
Source datasetuspto-grants-2002_09
ORD IDord-b1ce59aa907e44b3842890e5c899b0b2
Source noteuspto-grants-2002_09