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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638763Generated: November 2, 2026

Benzamide → N-Butylbenzamide

https://huagongshe.com/reaction/1638763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamideHCID 2331—
ReactantButyl bromideHCID 8002—
ReactantSodium HydroxideHCID 14798—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductN-ButylbenzamideHCID 76024—

Reaction Steps

1-Bromobutane (1.51 g, 0.011 mol) in benzene (10 ml) was slowly added to a refluxing mixture of benzamide (1.21 g, 0.01 mol), 50% aqueous sodium hydroxide solution (10 ml) and 1 mmol of the catalyst (Table 3). After the addition of has been completed, refluxing is continued for 4 hours. The reaction mixture was then cooled to room temperature and diluted with water (20 ml). The organic phase is separated, washed with water (3×10 ml) until neutral, dried over magnesium sulphate and evaporated to give pure N-n-butylbenzamide. Yields are given in Table 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880894
Source datasetuspto-grants-1989_11
ORD IDord-1517a2593f0c42d8aff2f9b3ccadd983
Source noteuspto-grants-1989_11