Chloride → HCID 25190241、化合物
反応式
[CH2:1]([O:3][C:4](=[O:18])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15](O)=[O:16])[CH3:2].[Cl-].O=S(Cl)Cl.Cl.[NH2:25][OH:26]>C(Cl)(Cl)Cl.ClCCl.N1C=CC=CC=1.C(OCC)(=O)C>[OH:26][NH:25][C:15](=[O:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:18]参加物
実験手順
In a single-neck flask equipped with reflux condenser, under stirring and argon flux, the 12-ethoxy-12-oxododecanoic acid (13; 1.5 g, 5.8 mmol) is solved in chloroform (20 mL). Thionyle chloride is dropped (SOCl2; 0.64 mL, 8.8 mmol) and the reaction is carried on under reflux for 3 h. The mixture is cooled down to room temperature and the solvent is eliminated under high vacuum. The obtained product is solved in dichloromethane (20 mL) and is added, at room temperature and under stirring, with a solution of hydroxylamine hydrochloride (0.61 g, 8.8 mmol) in pyridine (10 mL) leaving to react for 12 h under the same conditions. All the solvent are eliminated under high vacuum and the remaining product is solubilised in ethyl acetate (50 mL), washed with distilled water (3×20 mL). The organic phase is anhydrified with anhydrous sodium sulphate and filtered under vacuum. The solvent is evaporated and dried under high vacuum to give 1.3 g (Yield=82%) of product as a pale yellow solid.
後処理
- customIn a single-neck flask equipped
- temperaturewith reflux condenser
- temperatureunder reflux for 3 h
- additionis added, at room temperature
- customleaving
- customto react for 12 h under the same conditions
- washwashed with distilled water (3×20 mL)
- filtrationfiltered under vacuum
- customThe solvent is evaporated
- customdried under high vacuum
出典と根拠
- ORDレコード
- ord-dd5b592a288e439582a50d9f905114ae
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08816107B2
反応ノート
読み込み中…