反応式
F[C:2](S(OC)(=O)=O)(F)F.[OH:10][CH:11]([CH2:18][C:19]([O:21]CC)=O)[CH2:12][C:13](OCC)=[O:14].C(C1C=CC=C(C(C)(C)C)N=1)(C)(C)C.Cl>C(Cl)Cl.C1COCC1>[CH3:2][O:10][CH:11]([CH2:18][CH2:19][OH:21])[CH2:12][CH2:13][OH:14]参加物
反応条件
- 温度
- -5 °C
実験手順
25 ml of methyl trifluoromethylsulfonate are added to a solution of 30 g of diethyl 3-hydroxyglutarate and 33 ml of 2,6-di-tert-butylpyridine in 500 ml of DCM and the mixture is refluxed for 5 hours. After cooling, 500 ml of a 0.5N solution of HCl are added, the organic phase is decanted and dried over magnesium sulfate and the solvent is evaporated off under vacuum. The solid obtained is taken up with 200 ml of anhydrous THF, the mixture is filtered and the filtrate is then cooled to -5° C. 160 ml of a 1M solution of lithium aluminum hydride in THF are then added slowly and the mixture is stirred for 16 hours, the temperature being allowed to rise to RT. The reaction mixture is cooled to 0° C. and 5.5 ml of water, 18 ml of a 15% solution of NaOH and 5.5 ml of water are added successively. The mineral salts are filtered off and the filtrate is evaporated under vacuum to give the expected product after distillation under reduced pressure. B.p.=104° C. under 1.5 Pa.
後処理
- temperaturethe mixture is refluxed for 5 hours
- temperatureAfter cooling
- customthe organic phase is decanted
- dry with materialdried over magnesium sulfate
- customthe solvent is evaporated off under vacuum
- customThe solid obtained
- filtrationthe mixture is filtered
- addition160 ml of a 1M solution of lithium aluminum hydride in THF are then added slowly
- customto rise to RT
- temperatureThe reaction mixture is cooled to 0° C.
- addition5.5 ml of water, 18 ml of a 15% solution of NaOH and 5.5 ml of water are added successively
- filtrationThe mineral salts are filtered off
- customthe filtrate is evaporated under vacuum
出典と根拠
- ORDレコード
- ord-8afc1e24579042a999836fe21e456d14
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05618833
関連ノート
読み込み中…