反应 #4162610
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0a2440800ab340f288bed430bb4dd58f暂无可渲染的结构数据
C1=CC2=C(C=C1Br)C=C(O2)CO产品信息
(5-溴-1-苯并呋喃-2-基)甲醇(CAS 38220-77-8)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-0a2440800ab340f288bed430bb4dd58f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e51e18ea9634e0f87e8a265269d5d86反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6d5bb1f96c7d4295a75277454a382d4b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ecf9213e85ff4d188644431ac7c4171d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0a2440800ab340f288bed430bb4dd58f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e51e18ea9634e0f87e8a265269d5d86反应条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (5-bromo-benzofuran-2-yl)-methanol (1.6 g, 3.7 mmol) and 4-tert-butylstannanyl-pyridazine (1 g; 4.4 mmol) in 15 mL dry toluene, was added tetrakis(triphenylphosphine)palladium (0) (130 mg). The mixture was stirred at 95° C. overnight. After allowing the mixture to come to room temperature, the solution was poured into water, extracted, dried over MgSO4, and filtrated to afford 2.4 g of crude product that was further purified by chromatography to afford (5-pyridazin-4-yl-benzofuran-2-yl)-methanol. to come to room temperature extracted dried over MgSO4 filtrated to afford 2.4 g of crude product that was further purified by chromatography
来源 ID: ord-0f36db1a01f046d0ae021a045dd28b28反应条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (5-bromo-benzofuran-2-yl)-methanol (1 g, 4.4 mmol) and 2-tributylstannylpyrazine (1.6 g, 3.7 mmol) in 15 mL toluene at room temperature under argon, was added tetrakis(triphenylphosphine)palladium (0) (130 mg), and the mixture was heated at 95° C. overnight. The precipitate was allowed to cooled, extracted with ethyl acetate, washed with brine and dried over MgSO4. Filtration afforded 2.1 g of crude product that was further purified by chromatography to afford (5-pyrazin-2-yl-benzofuran-2-yl)-methanol. to cooled extracted with ethyl acetate washed with brine dried over MgSO4 Filtration afforded 2.1 g of crude product that was further purified by chromatography
来源 ID: ord-8837625675bf4aea9a2323603cb16c19反应条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (5-bromo-benzofuran-2-yl)-methanol (1 g, 4.4 mmol) and 2-tributylstannylpyrazine (1.6 g, 3.7 mmol) in 15 mL toluene at room temperature under argon, was added tetrakis(triphenylphosphine)palladium (0) (130 mg), and the mixture was heated at 95° C. overnight. The precipitate was allowed to cooled, extracted with ethyl acetate, washed with brine and dried over MgSO4. Filtration afforded 2.1 g of crude product that was further purified by chromatography to afford (5-pyrazin-2-yl-benzofuran-2-yl)-methanol. to cooled extracted with ethyl acetate washed with brine dried over MgSO4 Filtration afforded 2.1 g of crude product that was further purified by chromatography
来源 ID: ord-8837625675bf4aea9a2323603cb16c19反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of ethyl 5-bromo-benzofuran-2-carboxylate (5 g; 18.6 mmol) in 65 mL THF under nitrogen, was added DIBAL (46 mL, 46 mmol) dropwise over 30 minutes, then stirred overnight at room temperature. After dropwise addition of 25 mL of water, the mixture was evaporated, extracted with ethyl acetate, filtered, washed, dried (MgSO4) and evaporated to yield 4.2 g of crude product which was further purified by chromatography to afford (5-bromo-benzofuran-2-yl)-methanol. the mixture was evaporated extracted with ethyl acetate filtered washed dried (MgSO4) evaporated to yield 4.2 g of crude product which was further purified by chromatography
来源 ID: ord-f2e7841c5ebe4636a0f3340207c62eee反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6d5bb1f96c7d4295a75277454a382d4b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ecf9213e85ff4d188644431ac7c4171dPubChem References
以下资料来自该化合物的公开数据库参考记录。
