HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707378Generated: October 31, 2026
Potassium tert-butoxide → HCID 178509547, compound
https://huagongshe.com/reaction/1707378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178509745 | HCID 178509745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178509547 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05352795 |
|---|
| Source dataset | uspto-grants-1994_10 |
|---|
| ORD ID | ord-22dd19dd86514d3785df0314dc5e5fc0 |
|---|
| Source note | uspto-grants-1994_10 |
|---|