Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911548Generated: October 31, 2026

Ammonia → HCID 68712687, compound

https://huagongshe.com/reaction/1911548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-Fluoro-2-(trifluoromethyl)benzaldehydeHCID 522940—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
ProductHCID 68712687HCID 6871268781%

Reaction Steps

To a stirred solution of 4-fluoro-2-(trifluoromethyl)benzaldehyde (5.0 g) in methanol (20 ml) were added sequentially ammonia solution (28.9 ml, 7 M solution in methanol) and tetraisopropyl orthotitanate (9.0 ml) and the resulting mixture was stirred at r.t. for 1 h. Trimethylsilylcyanide (3.3 ml) was then added dropwise and stirring continued at r.t. overnight. The reaction mixture was poured onto ice-water (400 ml) and the mixture was then extracted twice with ethyl acetate. The combined organic phases were washed with brine and then dried over sodium sulphate and concentrated in vacuo to afford (RS)-amino-(4-fluoro-2-trifluoromethyl-phenyl)-acetonitrile (4.48 g, 81%) as an orange viscous oil. MS (ISP): 219.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-f610d3e1128c4c2c975dead96201334c
Source noteuspto-grants-2013_12