Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-(Methoxymethyl)-3-(trifluoromethyl)benzene | HCID 14926720 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22494069 | HCID 22494069 | — |
Reaction Steps
7.0 g of 1-(methoxymethyl)-3-(trifluoromethyl)benzene was dissolved in 300 ml anhydrous diethyl ether, and 19 ml n-butyl lithium (2.5 M solution in hexane) was added dropwise at −78° C. The reaction mixture was stirred at room temperature for 3 hours and cooled again at −78° C., and 10 ml N,N-dimethylformamide was added. The reaction solution was returned to room temperature, poured into water, extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evapoarated. The residue was subjected to silica gel column chromatography, and from fractions eluted with hexane-ethyl acetate (9:1), 5.0 g of 1-(methoxymethyl)-3-(trifluoromethyl)benzaldehyde was obtained as a reddish orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884821B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-468e933b6ee64bee857ce8cee8969f24 |
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| Source note | uspto-grants-2005_04 |
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