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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639683Generated: October 31, 2026

Benzeneacetonitrile, 4-methoxy- → HCID 25154238, compound

https://huagongshe.com/reaction/1639683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetonitrile, 4-methoxy-HCID 66031—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 63668480HCID 63668480—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 25154238HCID 2515423830%

Reaction Steps

To an ice-cooled and stirred mixture of 1-azido-2-chloro-4-trifluoromethyl-benzene (1.00 g, 1 eq) and commercial (4-methoxy-phenyl)-acetonitrile (0.797 g, 1.2 eq) in ethanol (10 ml) kept under nitrogen, a solution of sodium methoxide (0.366 g, 1.5 eq) in ethanol (10 ml) is added drop-wise (20 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 (40 ml), washed with water (2×50 ml), dried over MgSO4 and evaporated to dryness. The yellow solid residue (1.20 g) is purified by flash chromatography using 60-120 mesh silica gel and eluting with 15% ethylacetate in hexane, to afford the title compound as a white solid (0.324 g, 30% yield). M.p. 130.0-130.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110588B2
Source datasetuspto-grants-2012_02
ORD IDord-0a47f1852be64e6d8e9b7e60f349bfe4
Source noteuspto-grants-2012_02