Sodium Chloride → Arecoline
反応式
[CH3:1][N:2]1[CH2:7][C:6]([C:8]([O:10][CH3:11])=[O:9])=[CH:5][CH2:4][CH2:3]1.Br.[OH-].[K+].[Na+].[Cl-]>O>[CH3:1][N:2]1[CH2:7][C:6]([C:8]([O:10][CH3:11])=[O:9])=[CH:5][CH2:4][CH2:3]1参加物
5
実験手順
Ten grams of arecoline HBr was dissolved in a minimal quantity (approximately 25 ml) of water and adjusted to pH 10 with saturated KOH in a separatory funnel. One hundred mls of petroleum ether was added and the layers were mixed. NaCl was then added to saturate the aqueous layer. The organic layer was collected, and the aqueous layer was extracted three more times with petroleum ether. The combined organic layers were transferred to a 500 ml round bottom flask, boiling chips were added and the petroleum ether was removed by distillation. The remaining oil was layered with N2 and stored in low-actinic glassware. The oil was analyzed by NMR to show the absence of a halogen component.
後処理
- additionthe layers were mixed
- concentrationto saturate the aqueous layer
- customThe organic layer was collected
- extractionthe aqueous layer was extracted three more times with petroleum ether
- customThe combined organic layers were transferred to a 500 ml round bottom flask
- additionwere added
- customthe petroleum ether was removed by distillation
出典と根拠
- ORDレコード
- ord-d03f7efc0dae41fa989a1c73075a1399
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04965074
反応ノート
読み込み中…