Introduction of a new synthetic route about 3598-14-9

The synthetic route of Phenoxyacetonitrile has been constantly updated, and we look forward to future research findings.

A common heterocyclic compound, 3598-14-9, name is Phenoxyacetonitrile, molecular formula is C8H7NO, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. 3598-14-9.

To a stirring solution of the 2-[8-(benzyloxy)quinolin-7-yl]-l-phenylethanol(0.302 mmol) in phenoxyacetonitrile (9.05 mmol, 30 eq.) at -1O0C was dropwise added cone, sulfuric acid (1.51 mmol, 5.0 eq.). On completion of addition, the reaction mixture was allowed to warm to room temperature and was stirred 16h. The reaction was then diluted with ice that was allowed to melt and was then stirred 2h. The mixture was next brought to pH=7 by the addition of saturated aqueous sodium bicarbonate solution and then diluted with water (5 mL) and extracted with ethyl acetate (2 X 5 mL). The organic layers were combined, dried (MgSO4), filtered and concentrated to give sulfuric acid mono-{7-[2-(2- phenoxy-acetylamino)-2-phenyl-ethyl]-quinolin-8-yl} ester as a yellow oil that was purified by column chromatography using 20% methanol/dichloromethane. To a stirring suspension of the sulfuric acid mono-{7-[2-(2-phenoxy-acetylamino)-2-phenyl-ethyl]-quinolin-8-yl} ester (0.089 mmol, 1.0 eq.) from the initial step in methanol (9 mL) was added 3N HCl (18 mL) and the resulting suspension was heated to 550C and stirred 2h. The reaction mixture was then cooled to room temperature and organic solvents were removed by rotary evaporation resulting in a precipitate that was filtered yielding the pure product as a yellow solid (0.059 mmol, 12% for 2 steps). HRMS: calcd for C25H22N2O3 + H+, 399.17032; found (ESI-FTMS, [M+H]l+), 399.17059.

The synthetic route of Phenoxyacetonitrile has been constantly updated, and we look forward to future research findings.

Reference:
Patent; WYETH; WO2008/24922; (2008); A2;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts