Hydrochloric Acid → 4,5-difluoro-7-pentyl-2-(4-propylphenyl)-8,9-dihydro-7H-furo[3,2-f]chromene
反応式
[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[C:4](I)[C:3]=1[OH:19].C([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[CH2:28][CH2:29][CH3:30])#C.Cl.[CH2:32](N(CC)CC)[CH3:33]>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I>[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[C:4]2[CH:32]=[C:33]([C:26]3[CH:27]=[CH:22][C:23]([CH2:28][CH2:29][CH3:30])=[CH:24][CH:25]=3)[O:19][C:3]=12参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
2.0 g (5.23 mmol) of 7,8-difluoro-5-iodo-2-pentylchroman-6-ol are firstly stirred for 6 h at 60° C. together with 1.13 g (7.85 mmol) of ethynyl-n-propylbenzene in the presence of 110 mg (0.16 mmol) of bis(triphenylphosphine)palladium(II) chloride and 30 mg (0.16 mmol) of copper(I) iodide in 22 ml of triethylamine. The mixture is subsequently refluxed for 18 h. After cooling, the batch is added to ice/water and acidified using hydrochloric acid. The mixture is extracted a number of times with MTBE, and the combined extracts are washed with water and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2,
後処理
- temperatureThe mixture is subsequently refluxed for 18 h
- temperatureAfter cooling
- extractionThe mixture is extracted a number of times with MTBE
- washthe combined extracts are washed with water and sat. sodium chloride soln
- customThe solution is dried
- concentrationconcentrated to dryness
- customThe residue is purified by column chromatography (SiO2
出典と根拠
- ORDレコード
- ord-11954e2aaa5f443e9b83eafb4703cb91
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07678929B2
反応ノート
読み込み中…