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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580427Generated: October 30, 2026

Pyridine → HCID 13232127, compound

https://huagongshe.com/reaction/580427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzylamineHCID 7504—
Reactant2-(3,5-Dimethylphenoxy)butanoyl chlorideHCID 13232126—
SolventBenzeneHCID 241—
ProductHCID 13232127HCID 1323212762.1%

Reaction Steps

In 30 ml of benzene were dissolved 1.8 g (0.017 mole) of benzylamine and 1.2 g (0.015 mole) of pyridine, and thereto was added dropwise 3.0 g (0.013 mole) of 2-(3,5-dimethylphenoxy)-butyroyl chloride at room temperature with stirring. After the reaction was carried out for 5 hours, the reaction mixture was washed with water, dilute hydrochloric acid, dilute aqueous sodium hydroxide and then water successively. After the benzene layer was dried, the benzene was removed by distillation. The resultant crude crystals were recrystallized from n-hexane to give 2.4 g of N-benzyl-2-(3,5-dimethylphenoxy)-butyramide melting at 93°-94° C. as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753674
Source datasetuspto-grants-1988_06
ORD IDord-5c6aea464da4439da909422d134aaa9b
Source noteuspto-grants-1988_06