HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254482Generated: October 30, 2026
Trimethylsilyl cyanide → HCID 13511740, compound
https://huagongshe.com/reaction/254482
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 19743036 | HCID 19743036 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13511740 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07875645B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-932c2ebba1fa4b0bbbd13b6fc4a78aa6 |
|---|
| Source note | uspto-grants-2011_01 |
|---|