反応式
[CH2:1]([O:3][C:4]([CH:6]=P([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22]C=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:5])[CH3:2].[CH:26](N=C=S)(C)C.BrC(C)C(=O)C(OC)=O.O>C1COCC1>[CH3:20][CH2:25][CH2:24][CH:23]([CH3:22])[CH3:26].[C:4]([O:3][CH2:1][CH3:2])(=[O:5])[CH3:6]参加物
反応条件
- 温度
- -78 °C
実験手順
Ethoxycarbonylmethylene triphenyl phosphorane (33.8 g) in dry THF (200 ml) was treated with isopropyl isothiocyanate (10.1 g) at 65° C. for 16 h under nitrogen. The mixture was cooled to −78° C. and methyl 3-bromo-2-oxo-butanoate was added. The reaction was allowed to warm slowly to room temperature. After 24 h at room temperature more methyl 3-bromo-2-oxo-butanoate (2.8 g) was added and the mixture was warmed to 60° C. for 16 h. The cooled reaction was poured into water (1.5 L) and extracted into ether. Drying and evaporation gave an oil which was chromatographed (SiO2/10:1 isohexane-ethyl acetate then 5:1 isohexane-ethyl acetate) to afford the subtitle compound (23.5 g). δ 1HCDCl3 1.23-1.35 (9H, m), 2.26 (3H,s), 3.46 (1H, m), 3.82 (3H, s), 4.2 (2H, q), 7.42 (1H, br.s)
後処理
- temperatureto warm slowly to room temperature
- temperaturethe mixture was warmed to 60° C. for 16 h
- customThe cooled reaction
- extractionextracted into ether
- customDrying
- customevaporation
- customgave an oil which
- customwas chromatographed (SiO2/10:1 isohexane-ethyl acetate
出典と根拠
- ORDレコード
- ord-44497de50c15496f9245087358b694ec
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07384950B2
関連ノート
読み込み中…