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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707378Generated: October 31, 2026

Potassium tert-butoxide → HCID 178509547, compound

https://huagongshe.com/reaction/1707378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178509745HCID 178509745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178509547HCID 178509547—

Reaction Steps

A solution of potassium tert-butoxide (1.10 g) in tetrahydrofuran (50 mL) is added dropwise to a solution of 4-[1-(1,2,4-triazolyl) -5-chloropentyl]benzonitrile (2.50 g) in tetrahydrofuran at 0° (ice-bath). The reaction is allowed to proceed at 0° for 30 minutes and is then allowed to warm to room temperature during 3 hours. The reaction is then quenched with water (100 mL) and the mixture is subsequently extracted with ethyl acetate (100 mL). The organic extract is extracted with 3 N hydrochloric acid (3×30 mL) and the combined acid extracts are made basic with 6 N sodium hydroxide. The crude product is extracted into ethyl acetate (3×30 mL) and the combined extracts are dried (MgSO4) and evaporated to afford 1-(4-cyanophenyl)-1-(1,2,4-triazolyl)cyclopentane. The compound is dissolved in acetone and treated with ethereal HCl to afford the hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05352795
Source datasetuspto-grants-1994_10
ORD IDord-22dd19dd86514d3785df0314dc5e5fc0
Source noteuspto-grants-1994_10