反応式
Br[C:2]1[C:6]([Br:7])=[CH:5][S:4][CH:3]=1.C([Li])CCC.CN(OC)[C:15](=[O:18])[CH2:16][CH3:17]>CCOCC>[Br:7][C:6]1[C:2]([C:15](=[O:18])[CH2:16][CH3:17])=[CH:3][S:4][CH:5]=1参加物
実験手順
A solution of 3,4-dibromothiophene (6.0 g, 24.8 mmol) in 10 mL of ether was cooled to -78° C. and trated with n-butyllithium (9.92 mL, 2.5M solution in hexanes, 24.8 mmol). While holding the temperature at -78° C., the reaction was stirred for 15 minutes, then 2.9 g (24.8 mmol) of N-methyl-N-methoxypropionamide was added and the reaction was stirred for 1 hour. The reaction was quenched with satd NH4Cl, and the mixture was diluted with ether. The ether layer was separated, washed with water and brine, dried over MgSO4 and concentrated. The residue was triturated with hexanes, and the mixture was filtered. The solvent was removed to give 2.08 g of a tan solid. MS 236, 238 (M+NH4)+. NMR (CDCl3) δ:7.99 (d, J=3 Hz, 1H), 7.32 (d, J=3 Hz, 1H), 2.98 (q, J=7 Hz, 2H), 1.21 (t, J=7 Hz, 3H).
後処理
- customat -78° C.
- stirringthe reaction was stirred for 1 hour
- customThe reaction was quenched with satd NH4Cl
- additionthe mixture was diluted with ether
- customThe ether layer was separated
- washwashed with water and brine
- dry with materialdried over MgSO4
- concentrationconcentrated
- customThe residue was triturated with hexanes
- filtrationthe mixture was filtered
- customThe solvent was removed
出典と根拠
- ORDレコード
- ord-a348106b0b6d43e3a45bb6ec8506f1c4
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05597832
関連ノート
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