Diethyl Ether → 2,4-Dimethylthiophene-3-carbaldehyde
反応式
[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH3:8])[C:6]=1Br.C[CH2:10][O:11]CC.C([Li])CCC.CN(C)C=O>CCCCCC>[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH3:8])[C:6]=1[CH:10]=[O:11]参加物
6
反応条件
- 温度
- -20 °C
実験手順
A solution of 15 g. (79.0 mmol) of 2,4-dimethyl-3-bromothiophene in 120 ml. of dry ether was cooled to -70° C. and 36 ml. of a hexane solution of n-butyl lithium (2.4 molar, 86.4 mmol) were added dropwise. The reaction mixture was allowed to warm up to -20° C. for 10 min., cooled again to -70° C. and then quenched by adding dropwise 15 g. (0.205 mol) of dimethylformamide. The mixture was stirred at room temperature overnight, poured into ice water, stirred for 15 min. and extracted four times with ether. The ether phase was washed with saturated sodium chloride solution, dried and evaporated. The resulting oily residue was distilled to yield 2,4-dimethylthiophene-3-carboxaldehyde, b.p. 50°-55° C./0.1 mm.
後処理
- temperaturecooled again to -70° C.
- customquenched
- additionby adding dropwise 15 g
- stirringstirred for 15 min.
- extractionextracted four times with ether
- washThe ether phase was washed with saturated sodium chloride solution
- customdried
- customevaporated
- distillationThe resulting oily residue was distilled
出典と根拠
- ORDレコード
- ord-3ebb462a37434efc8c3903babe0579c1
- 出典データセット
- uspto-grants-1980_10
- 特許番号
- US04230872
反応ノート
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