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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275998Generated: October 26, 2026

Pyridine → N-butyl-N-(3-hydroxymethylphenyl)-bromoacetamide

https://huagongshe.com/reaction/1275998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetyl bromideHCID 61147—
Reactant[3-(Butylamino)phenyl]methanolHCID 22322603—
SolventTolueneHCID 1140—
ProductN-butyl-N-(3-hydroxymethylphenyl)-bromoacetamideHCID 22323007—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3.42 g (19.2 mmol) of the compound of Example 532A in 20 ml toluene, was added 2.42 ml (30 mmol) pyridine. The mixture was cooled to 0° C.; 4.025 gm (20.0 mmol) of bromoacetyl bromide (diluted with 5 ml toluene) was added in a dropwise fashion. The reaction mixture was allowed to stir for 5 hours at 0° C. and then was allowed to warm to room temperature. Saturated potassium carbonate solution was added, and the mixture was stirred vigorously for 2 hours. The mixture was extracted with EtOAc; the organic layer was washed with 1N H3PO4, water, and brine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162927
Source datasetuspto-grants-2000_12
ORD IDord-a12f475ab6d6437bb1d940f32dd67f4f
Source noteuspto-grants-2000_12