Methane, dichloromethoxy- → 4-Fluoro-1-methoxy-2-naphthaldehyde
反応式
[CH3:1][O:2][CH:3](Cl)Cl.[Sn](Cl)(Cl)(Cl)Cl.[F:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:15]([O:22]C)=[CH:14][CH:13]=1>ClCCl>[F:11][C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:3]([O:2][CH3:1])=[C:14]([CH:15]=[O:22])[CH:13]=1参加物
反応条件
- 温度
- 5 °C
実験手順
5.25 ml of dichloromethyl methyl ether were dissolved in 40 ml dichloromethane and cooled to +5° C. 6.75 ml tin(IV)chloride were added neat over 45 min to the solution. After the addition the mixture was stirred for 45 min at 5° C. 11.4 g 4-fluoro-1-methoxy-naphthalene in 30 ml dichloromethane was added over 1 h. Then the cooling bath was removed, and the mixture was stirred for 2 h at ambient temperature. It was then poured into ice/water. The dichloromethane layer was separated and the aqueous phase was extracted with dichloromethane. The combined dichloromethane layers were washed with water, dried over sodium sulfate, filtered through celite and concentrated in vacuo. The residue was treated with pentane to yield 9.3 g of 4-fluoro-1-methoxynaphthalene-2-carbaldehyde as a brown solid.
後処理
- temperaturecooled to +5° C
- additionAfter the addition the mixture
- customThen the cooling bath was removed
- stirringthe mixture was stirred for 2 h at ambient temperature
- additionIt was then poured into ice/water
- customThe dichloromethane layer was separated
- extractionthe aqueous phase was extracted with dichloromethane
- washThe combined dichloromethane layers were washed with water
- dry with materialdried over sodium sulfate
- filtrationfiltered through celite and
- concentrationconcentrated in vacuo
- additionThe residue was treated with pentane
出典と根拠
- ORDレコード
- ord-9ca8de85420f47bc8c98ca8615aeb720
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08501981B2
反応ノート
読み込み中…