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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280484Generated: October 30, 2026

1,3-Propanediamine → n-(3-Aminopropyl)benzamide

https://huagongshe.com/reaction/1280484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediamineHCID 428—
ReactantBenzamideHCID 2331—
Productn-(3-Aminopropyl)benzamideHCID 23899333.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

Benzamide (25 g, 0.20 mol) and 1,3-diaminopropane (45.9 g, 0.60 mol) were combined in a Parr vessel and heated to 150° C. for 15 hours. The vessel was cooled and the reaction mixture was concentrated under vacuum to remove excess diamine. The residue was dissolved in water (500 mL) and concentrated hydrochloric acid was added to adjust the pH to <1. The resulting precipitate (starting benzamide and diacylated product) was removed by filtration. The filtrate was washed with dichloromethane. The aqueous layer was made strongly basic by the addition of 50% sodium hydroxide and then it was extracted with dichloromethane (4×300 mL). The extracts were combined, washed with brine (300 mL), dried over sodium sulfate and then concentrated under vacuum to provide 11.9 g of N-(3-aminopropyl)benzamide as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451810B1
Source datasetuspto-grants-2002_09
ORD IDord-f1bb97e8910b4f009c2284bb5740864a
Source noteuspto-grants-2002_09