Acetyl chloride → L-Norvaline, methyl ester
反応式
[C:1](Cl)(=O)C.[NH2:5][C@H:6]([C:10]([OH:12])=[O:11])[CH2:7][CH2:8][CH3:9]>CO>[CH3:1][O:11][C:10](=[O:12])[C@H:6]([CH2:7][CH2:8][CH3:9])[NH2:5]参加物
4
実験手順
To 20 mL of methanol was slowly added 2.6 mL acetyl chloride. Then 2.0 g (17.1 mmole) of L-norvaline was added. The solution was heated to reflux and monitored by thin-layer chromatography (TLC) until complete. The methanol was stripped off by rotary evaporation and the resulting oil was pumped under high vacuum overnight to give the title compound. NMR(300 MHZ, CD3OD): δ 4.03 (t, Nva-α, 1H), 3.81 (s, COOCH3, 3H), 1.87 (m, CH2CH2CH3, 2H), 1.44 (m, CH2CH2CH3, 2H), 0.98 (t, CH2CH2CH3, 3H).
後処理
- temperatureThe solution was heated
- temperatureto reflux
- customThe methanol was stripped off by rotary evaporation
- customwas pumped under high vacuum overnight
出典と根拠
- ORDレコード
- ord-d038bcdebc68470bb7cdd8f58e0a9df3
- 出典データセット
- uspto-grants-1998_02
- 特許番号
- US05719296
反応ノート
読み込み中…