Triethylamine → (S)-Methyl morpholine-3-carboxylate
反応式
C(N(CC)CC)C.[CH3:8][O:9][C:10](=[O:18])[C@@H:11]([NH2:17])[CH2:12][O:13][CH2:14][CH2:15]Cl>CO>[CH3:8][O:9][C:10]([C@@H:11]1[CH2:12][O:13][CH2:14][CH2:15][NH:17]1)=[O:18]参加物
4
実験手順
Triethylamine (1.2 mL) was added to the above-obtained (2S)-2-amino-3-(2-chloroethoxy)propanoic acid methyl ester (726 mg) in methanol (10 mL), and the resultant mixture was refluxed under heat for 3 hours, and then cooled in air. The reaction solvent was removed under reduced pressure. Ethyl acetate was added to the residue, and insoluble matter was removed by filtration. The solvent of the filtrate was removed under reduced pressure, to thereby give the title compound as an oily product (467 mg, 80%).
後処理
- temperatureunder heat for 3 hours
- temperaturecooled in air
- customThe reaction solvent was removed under reduced pressure
- additionEthyl acetate was added to the residue, and insoluble matter
- customwas removed by filtration
- customThe solvent of the filtrate was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-1e69003d772f40dcaa0000907fd03886
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07622471B2
反応ノート
読み込み中…