Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639685Generated: November 1, 2026

Benzeneacetonitrile, 4-methoxy- → HCID 25215442, compound

https://huagongshe.com/reaction/1639685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetonitrile, 4-methoxy-HCID 66031—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 43154606HCID 43154606—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 25215442HCID 2521544234.1%

Reaction Steps

To an ice-cooled and stirred mixture of 1-azido-2-chloro-4-fluoro-benzene (0.300 g, 1 eq) and commercial (4-methoxy-phenyl)-acetonitrile (0.309 g, 1.2 eq) in ethanol (5 ml) kept under nitrogen, a solution of sodium methoxide (0.142 g, 1.5 eq) in ethanol (5 ml) is added drop-wise (15 min). After the addition, the reaction mixture is allowed to reach room temperature spontaneously and stirring is then continued overnight at room temperature. The resulting reaction mixture is diluted with ethyl acetate (20 ml), washed with water (2×25 ml), dried over MgSO4 and evaporated to dryness. The yellow semisolid residue (˜0.500 g) is purified by flash chromatography using 60-120 mesh silica gel and eluting with 20% ethylacetate in hexane, to afford the title compound as a white solid (0.190 g, 34% yield). M.p. 136.3-141.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110588B2
Source datasetuspto-grants-2012_02
ORD IDord-a617c825dc354df38a0e66c874090241
Source noteuspto-grants-2012_02