Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040321Generated: October 29, 2026

Potassium tert-butoxide → 4-(Methoxymethyl)cyclohexanecarbonitrile

https://huagongshe.com/reaction/2040321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantToluenesulfonylmethyl isocyanideHCID 53627694—
Reactant4-(Methoxymethyl)cyclohexan-1-oneHCID 57829016—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(Methoxymethyl)cyclohexanecarbonitrileHCID 67126819—

Reaction Steps

To a cold (−10° C.) solution of EXAMPLE 374C (1.18 g) and toluenesulfonylmethyl isocyanide (2.268 g) in dimethoxyethane (3 mL) and absolute ethanol (0.1 mL) was added (in small portions) potassium tert-butoxide (2.235 g). The reaction mixture was continued to stir at <5° C. for 30 minutes, warmed to room temperature, heated at 35° C. for 30 minutes and then at room temperature for 2 hours. The reaction mixture was concentrated and the residue was dissolved in water-brine, and extracted with dichloromethane. The dichloromethane layer was purified by flash chromatography, and was eluted with 5% ethyl acetate in dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580794B2
Source datasetuspto-grants-2013_11
ORD IDord-49b10596bf6c48519497e071bc4119ff
Source noteuspto-grants-2013_11