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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388848Generated: November 2, 2026

4-Hydroxybenzaldehyde → p-Formylphenyl 1-amidino-4-piperidinepropionate hydrochloride

https://huagongshe.com/reaction/1388848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Amidino-4-piperidinepropionic acid hydrochlorideHCID 15583512—
SolventPyridineHCID 1049—
Productp-Formylphenyl 1-amidino-4-piperidinepropionate hydrochlorideHCID 8673927936.4%

Reaction Steps

A mixture of 4.0 g of 1-amidino-4-piperidinepropionic acid hydrochloride and 2.1 g of p-hydroxybenzaldehyde was suspended in 20 ml of dry pyridine. 3.5 g of dicyclohexylcarbodiimide was added with stirring to the suspension, and the resulting mixture was stirred overnight at room temperature. After removal of any insoluble materials, the filtrate was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was stirred to give crystals. The crystals were recrystallized from methanol-ether to obtain 2.1 g (yield: 36.4%) of p-formylphenyl 1-amidino-4-piperidinepropionate hydrochloride as colorless crystals having a melting point of 144° to 147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04433152
Source datasetuspto-grants-1984_02
ORD IDord-5af6023b70d844b9b134f63e8d5cff30
Source noteuspto-grants-1984_02