HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892144Generated: October 29, 2026
3-[(2-Methoxyethoxy)methoxy]benzaldehyde → 1-(2-Methoxyethoxy)-methoxy-3-(2-quinolin-2-yl-vinyl)-benzene
https://huagongshe.com/reaction/892144
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-[(2-Methoxyethoxy)methoxy]benzaldehyde | HCID 15755175 | — |
| Reactant | Triphenyl[(quinolin-2-yl)methyl]phosphanium chloride | HCID 22241267 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Methoxyethoxy)-methoxy-3-(2-quinolin-2-yl-vinyl)-benzene | HCID 54407582 | — |
Reaction Steps
To a cooled (−78° C.) suspension of triphenyl-(quinolin-2-yl-methyl)-phosphonium chloride (1.76 g, 4 mmol, example 17) in THF (24 mL) is added, dropwise, n-butyl lithium solution (1.7 mL, 2.5 M in hexanes). The resulting mixture is stirred for 30 min. then a solution of 3-[(2-methoxyethoxy)-methoxy]-benzaldehyde (756 mg, 3.6 mmol, example 8a) in THF (3 mL) is added. This mixture is stirred for 30 min then the cold bath removed and stirring continued for 2 h. The reaction mixture is then diluted with ethyl acetate, washed with sat. ammonium acetate solution and brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (silica, 40% ethyl acetate in hexanes) to give the title compound as an oil. MS (ESI) 336 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005440B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-1f4301884b474332aafc444fae97cc31 |
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| Source note | uspto-grants-2006_02 |
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