Acetaldehyde → HCID 61695367、化合物
反応式
Cl.C([O:4][C:5](=[O:8])[CH2:6][NH2:7])C.CC[N:11]([CH2:14][CH3:15])CC.[CH:16](=O)[CH3:17].[Si](C#N)(C)(C)[CH3:20]>C(Cl)Cl>[CH2:16]([N:7]([CH:15]([C:14]#[N:11])[CH3:20])[CH2:6][C:5]([OH:4])=[O:8])[CH3:17]参加物
実験手順
To a suspension of glycine ethyl ester hydrochloride (3.0 g, 0.021 mol) in DCM (80 mL) was added Et3N (3.0 mL, 0.021 mol). The resulting mixture was stirred at room temperature for 10 minutes, then acetaldehyde (1.2 mL, 0.021 mol) was added, followed by the drop-wise addition of TMSCN (2.86 mL, 0.021 mol). The resulting homogeneous solution was stirred at room temperature for 18 hours, then was diluted with DCM (100 mL) and washed with brine (100 mL), dried (Na2SO4), and concentrated in vacuo. The crude mixture was purified by flash column chromatography on silica gel (7:3 EtOAc/hexane). The title compound (3.5 g, 87%) was isolated as its white, solid, hydrochloride salt. TLC Rf (free base) 0.8 (EtOAc). 1H NMR (methanol-d4) δ1.34 (t, J=7.2 Hz, 3H), 1.73 (d, J=7.2 Hz, 3H), 4.16 (d, J=4 Hz, 2H), 4.33 (q, J=7.2 Hz, 2H), 4.70 (q, J=7.2 Hz, 1H).
後処理
- stirringThe resulting homogeneous solution was stirred at room temperature for 18 hours
- washwashed with brine (100 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- customThe crude mixture was purified by flash column chromatography on silica gel (7:3 EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-a822c3c460fa46299819093699a10585
- 出典データセット
- uspto-grants-2003_01
- 特許番号
- US06506761B1
反応ノート
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