Hydrochloric Acid → 4,5-difluoro-7-pentyl-2-(4-propylphenyl)-8,9-dihydro-7H-furo[3,2-f]chromene
반응식
[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]=12참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
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,
후처리
- 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
출처 및 근거
- ORD 기록
- ord-11954e2aaa5f443e9b83eafb4703cb91
- 출처 데이터셋
- uspto-grants-2010_03
- 특허 번호
- US07678929B2
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