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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254482Generated: October 30, 2026

Trimethylsilyl cyanide → HCID 13511740, compound

https://huagongshe.com/reaction/254482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 19743036HCID 19743036—
SolventAcetonitrileHCID 6342—
ProductHCID 13511740HCID 13511740—

Reaction Steps

7.36 g (74.4 mmol) Trimethylsilyl cyanide was added to a solution of 74.4 ml (1.0 M in THF, 74.4 mmol) tetrabutylammonium flouride in 300 ml acetonitrile and the mixture was stirred for 5 minutes. 5.28 g (24.8 mmol) rac-1-(1-Bromo-propyl)-4-methylbenzene were added and the reaction mixture was stirred at ambient temperature for 16 hours. The solvent was removed in vacuo and the viscous residue obtained was partitioned between water and dichloromethane. The dichloromethane was separated, then washed with water, dried over MgSO4 and evaporated to dryness. Purification of the residue by column chromatography on silica gel with a gradient of heptane to 9:1 heptane/ethyl acetate afforded rac-2-p-tolyl-butyronitrile as a colourless oil. NMR (CDCl3, ppm): 0.95 (3H, t), 1.77 (2H, m), 2.21 (3H, s), 3.58 (1H, t), 7.07 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875645B2
Source datasetuspto-grants-2011_01
ORD IDord-932c2ebba1fa4b0bbbd13b6fc4a78aa6
Source noteuspto-grants-2011_01