Sodium Hydroxide → 3-Aminoazepan-2-one hydrochloride
反応式
[ClH:1].[NH2:2][C@H:3]([C:9]([OH:11])=O)[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8].[OH-].[Na+]>C(O)CCCCC>[ClH:1].[NH2:2][CH:3]1[CH2:4][CH2:5][CH2:6][CH2:7][NH:8][C:9]1=[O:11]参加物
4
実験手順
A stirred mixture of L-lysine hydrochloride 1 (55 g, 300 mmol) and NaOH (12 g, 300 mmol) in hexanol (1.2 L) is heated to reflux with a Dean-Stark trap used to remove H2O. The suspension is refluxed for 8 hours until all starting material is consumed (which maybe determined by 1 H NMR). The suspension is then cooled and filtered to remove byproduct NaCl. The filtrate is concentrated and the resulting crude α-amino-ε-caprolactam 2 is dissolved in water. After acidification to pH 6 with addition of concentrated HCl and partial concentration, crystals maybe formed at room temperature to afford α-amino-εcaprolactam hydrochloride (37 g) in 75% yield.
後処理
- temperatureis heated
- temperatureto reflux with a Dean-Stark trap
- customto remove H2O
- temperatureThe suspension is refluxed for 8 hours until all starting material
- customis consumed (which
- temperatureThe suspension is then cooled
- filtrationfiltered
- customto remove byproduct NaCl
- concentrationThe filtrate is concentrated
- dissolutionthe resulting crude α-amino-ε-caprolactam 2 is dissolved in water
- additionAfter acidification to pH 6 with addition of concentrated HCl and partial concentration, crystals
- custommaybe formed at room temperature
出典と根拠
- ORDレコード
- ord-c493eb10334c4796b6bef3f1d3aa436f
- 出典データセット
- uspto-grants-2008_07
- 特許番号
- US07399855B2
反応ノート
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