反応 #4162610
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a2440800ab340f288bed430bb4dd58f表示可能な構造データがありません
C1=CC2=C(C=C1Br)C=C(O2)CO製品情報
(5-bromo-1-benzofuran-2-yl)methanol (CAS 38220-77-8) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 2795537
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a2440800ab340f288bed430bb4dd58f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3e51e18ea9634e0f87e8a265269d5d86反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6d5bb1f96c7d4295a75277454a382d4b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ecf9213e85ff4d188644431ac7c4171d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0a2440800ab340f288bed430bb4dd58f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3e51e18ea9634e0f87e8a265269d5d86反応条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-0f36db1a01f046d0ae021a045dd28b28反応条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-8837625675bf4aea9a2323603cb16c19反応条件: temp:95.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-8837625675bf4aea9a2323603cb16c19反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-f2e7841c5ebe4636a0f3340207c62eee反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6d5bb1f96c7d4295a75277454a382d4b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ecf9213e85ff4d188644431ac7c4171dPubChem References
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