反応式
C1(P(C2C=CC=CC=2)(S)=[S:8])C=CC=CC=1.[CH2:16]([O:18][C:19](=[O:24])[CH:20]([C:22]#[N:23])[CH3:21])[CH3:17].CCOC(C)=O>C(O)(C)C>[NH2:23][C:22](=[S:8])[CH:20]([CH3:21])[C:19]([O:18][CH2:16][CH3:17])=[O:24]参加物
実験手順
A mixture of diphenylphosphinodithioic acid (ALFAAESAR, 37.4 g, 149 mmol) and 2-cyanopropionic acid ethyl ester (ABCR, 9.90 mL, 74.7 mmol) in isopropanol (350 mL) was heated under reflux for 5 h. TLC (Hex:EtOAc 7:3) showed reaction had gone to completion. Reaction mixture was allowed to cool and was placed in the fridge overnight. Reaction mixture was filtered off and washed with isopropanol. Residue was partitioned between ethyl acetate (250 mL) and 1N NaOH (250 mL). Phases were separated and organic phase was washed with water (300 mL), brine (300 mL), dried over sodium sulfate and concentrated to dryness. Crude was purified by chromatography on silica gel using a hexane/EtOAc gradient. Appropriate fractions were combined and evaporated to yield title compound as a white solid (6.6 g, 40.9 mmol, 54.8% yield). 1H NMR (300 MHz, DMSO-d6) δ ppm: 9.60 (s, 1H), 9.40 (s, 1H), 4.05 (q, 2H), 3.74 (q, 1H), 1.29 (d, 3H), 1.15 (t, 3H). [ES+MS] m/z 162 (MH+).
後処理
- temperaturewas heated
- temperatureunder reflux for 5 h
- customreaction
- customReaction mixture
- temperatureto cool
- customwas placed in the fridge overnight
- customReaction mixture
- filtrationwas filtered off
- washwashed with isopropanol
- customResidue was partitioned between ethyl acetate (250 mL) and 1N NaOH (250 mL)
- customPhases were separated
- washorganic phase was washed with water (300 mL), brine (300 mL)
- dry with materialdried over sodium sulfate
- concentrationconcentrated to dryness
- customCrude was purified by chromatography on silica gel using a hexane/EtOAc gradient
- customevaporated
出典と根拠
- ORDレコード
- ord-b08789d4b8364c468562b26294cbcc5b
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US09000181B2
関連ノート
読み込み中…