HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639683Generated: October 31, 2026
Benzeneacetonitrile, 4-methoxy- → HCID 25154238, compound
https://huagongshe.com/reaction/1639683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 63668480 | HCID 63668480 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25154238 | HCID 25154238 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110588B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-0a47f1852be64e6d8e9b7e60f349bfe4 |
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| Source note | uspto-grants-2012_02 |
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