Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985108Generated: October 30, 2026

Potassium Hydroxide → 1-(3-Bromophenyl)cyclohexanecarboxamide

https://huagongshe.com/reaction/1985108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 43345643HCID 43345643—
Solventtert-ButanolHCID 6386—
Product1-(3-Bromophenyl)cyclohexanecarboxamideHCID 58909432—

Reaction Steps

With overhead stirrer, a mixture of crude product from step 1, above, (380 g, 1207 mmol), powdered KOH (720 g) and t-BuOH (2.5 L) was heated at reflux overnight. See Hall, J. H.; Gisler, M. A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol. J. Org. Chem. 1976, 41, 3769-3770. If deemed complete by GC analysis, it was cooled with ice-water (cool slowly to avoid shock to the glass), quenched with ice-water (1500 mL). The quenched mixture was then extracted with MTBE (3.5 L+1.5 L). MTBE layers were concentrated to a yellow solid, 390 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544717B2
Source datasetuspto-grants-2009_06
ORD IDord-3cedd4ad77404918b787e475270c4ca1
Source noteuspto-grants-2009_06