反应 #4164487
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d7307667a8544e239931ac11aa273277暂无可渲染的结构数据
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isothiocyanatomethylbenzene(CAS 622-78-6)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d7307667a8544e239931ac11aa273277反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c61a766e0c24483787686d514c0b8c18反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a6aa58f1effa4c4d8a924bcfc2c633d0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-491fcab3a1d8442192dda6cac0a3b0aa反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d6d117a72b541f28f12cb74dd15fe60反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7032b657091141bfab6c9b2229495d86反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bc532156e6d94cf18fba1a9dd6677730反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-913eab88a461495b9e52202d676e3275反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-021e2724be8a466e8c23ed0de347db24反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-be10d8b6b5324f398090d0010566be0e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione (0.4 g) in anhydrous tetrahydrofuran (10 ml) was added benzyl isothiocyanate (0.24 g) and the mixture was stirred at room temperature for 5.5 hours and then at 50° C. for 9 hours. The reaction mixture was concentrated. The residue was chromatographed on a silica gel column using ethyl acetate:n-hexane=1:1→3:1 as the eluant to afford the title compound (0.36 g, Rf=0.53: thin layer chromatography on a silica gel plate using ethyl acetate:n-hexane=3:1). at 50° C. for 9 hours The reaction mixture was concentrated The residue was chromatographed on a silica gel column
来源 ID: ord-f2920676c5d5441f87a7bf7e8e1c8e95反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 5-[4-[6-(4-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (400 mg), benzyl isothiocyanate (248 mg), triethylamine (153 mg) and anhydrous N,N-dimethylformamide (8 ml) was stirred at room temperature for 3.5 hours. The reaction mixture was concentrated and partitioned between ethyl acetate and water. The extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and then concentrated. The residue was chromatographed on a silica gel column using ethyl acetate:n-hexane=2:1→3:1→4:1 as the eluant to afford the title compound (291 mg, mp 174.8-177.2° C.). The reaction mixture was concentrated partitioned between ethyl acetate and water The extract was washed with saturated aqueous sodium chloride solution dried over anhydrous sodium sulfate concentrated The residue was chromatographed on a silica gel column
来源 ID: ord-db4b82b32c26403a8ca054c4579ac06dPubChem References
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