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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831927Generated: November 1, 2026

Trimethylsilyl cyanide → Methyl 3-(cyanomethyl)benzoate

https://huagongshe.com/reaction/1831927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantMethyl 3-(bromomethyl)benzoateHCID 517981—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-(cyanomethyl)benzoateHCID 1082113643%

Reaction Steps

To an ice-cold solution of methyl 3-bromomethylbenzoate (9.1 g, 40 mmol) in CH3CN (108 mL) was added tetrabutylammonium fluoride (17.3 mL, 60 mmol) and trimethylsilylcyanide (8.0 mL, 60 mmol), and the reaction mixture was heated at reflux for 20 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure. Purification by flash column chromatography (silica, 1:1 EtOAc/hexanes) provided methyl 3-cyanomethylbenzoate as a clear oil (3.0 g, 43%): 1H NMR (300 MHz, DMSO-d6) δ 7.97 (s, 1H), 7.92 (d, J=8 Hz, 1H), 7.64 (d, J=8 Hz, 1H), 7.56 (t, J=8 Hz, 1H), 4.16 (s, 2H), 3.87 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-ac9f7fff663a43a0a83b62638263b3ff
Source noteuspto-grants-2006_06