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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433258Generated: November 1, 2026

Potassium Hydroxide → 6-(But-3-en-1-yloxy)hexanenitrile

https://huagongshe.com/reaction/1433258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-Buten-1-olHCID 69389—
Reactant6-BromohexanenitrileHCID 81093—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-(But-3-en-1-yloxy)hexanenitrileHCID 57933189—

Reaction Steps

6-Bromocapronitrile (1.19 ml, 9.00 mmol) and 3-buten-1-ol (946 ul, 11.0 mmol) were added to a stirred solution of potassium hydroxide (6.16 g, 110 mmol) and tetra-butylammonium bromide (434 mg, 1.35 mmol) in water (6 ml) and dichloromethane (2 ml). The reaction was stirred at room temperature for 4 days and then washed with diethyl ether (2×50 ml). The combined organics were washed with water (3×30 ml), dried (magnesium sulphate) and the solvent removed in vacuo to furnish the title compound as a colourless oil, 1.48 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612084B2
Source datasetuspto-grants-2009_11
ORD IDord-98a6237eaba5469894b2f07f624b0954
Source noteuspto-grants-2009_11