反应 #4153279
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6b5d3d161a584883ae444e35f5a0899d暂无可渲染的结构数据
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2,6-二氟-4-羟基苯腈(CAS 123843-57-2)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-6b5d3d161a584883ae444e35f5a0899d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e641ce8c83314945be60c04c47df8740反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c482039bb42a418e824987129af809bf反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ea107c01c214e6ab5e40d256b1ade75反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1629e6f167c4ba287f0f8fdc1a28a60反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9deb8edefe4e432983e052ba60730012反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e8b7cc171bdc4a59b2d7585fc5477f57反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6b5d3d161a584883ae444e35f5a0899d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Then, 1.1 g (6.4 mmol) of 2,6-difluoro-4-hydroxybenzo-nitrile, 0.8 ml of pyridine, and 2 ml of toluene were mixed. To this mixture, was added dropwise 3 ml of toluene solution containing 6.4 mmol of 2-fluoro-4-(2-(trans-4-pentylcyclohexyl)ethyl)benzoyl chloride at room temperature in 5 minutes. After the dropping was finished, they were reacted at 50° C. for 2 hours. After finishing of the reaction, 10 ml of water was added to the reaction product, and then extracted with 30 ml of toluene. The organic layer thus obtained was washed with 6N-hydrochloric acid thrice, 2N-sodium hydroxide thrice, and water thrice, and then dried over anhydrous magnesium sulfate. Solvent was distilled off at a reduced pressure, and the residue was subjected to a silica gel column chromatography (eluent: toluene) to obtain 2.8 g of a crude 3,5-difluoro-4-cyanophenyl 2-fluoro-4-(2-(trans-4-pentylcyclohexyl)ethyl)benzoate. This product was recrystallized from a mixed solvent of heptane/ether to obtain 2.4 g of (yield: 81.6%) the subject compound. they were reacted at 50° C. for 2 hours was added to the reaction product extracted with 30 ml of toluene The organic layer thus obtained was washed with 6N-hydrochloric acid thrice, 2N-sodium hydroxide thrice, and water thrice dried over anhydrous magnesium sulfate Solvent was distilled off at a reduced pressure
来源 ID: ord-3c1a33884f244ffdbba787a6d3ffa690反应条件: temp:180.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A stirred, homogeneous mixture of finely powdered, compound 27 (17.0 g, 0.10 mol), aluminium chloride (29.4 g, 0.22 mol) and sodium chloride (7.1 g, 0.12 mol) was heated to 180° C. over 25 min and then at 180° C. for 1 h (glc and tlc analyses both revealed a complete reaction). Ice-water was added, and the product was extracted into ether (twice). The combined ethereal extracts were washed with water, and the product was extracted into 10% sodium hydroxide (twice) and the combined basic extracts were acidified with 36% hydrochloric acid. The product was extracted into ether (twice), and the combined ethereal extracts were washed with water and dried (MgSO4). The solvent was removed in vacuo to give a fawn solid. a complete reaction) the product was extracted into ether (twice) The combined ethereal extracts were washed with water the product was extracted into 10% sodium hydroxide (twice) and the combined basic extracts The product was extracted into ether (twice), and the combined ethereal extracts were washed with water dried (MgSO4) The solvent was removed in vacuo to give a fawn solid
来源 ID: ord-2f4bdb0a3888460ea89a01d4ed7a2a69反应条件: temp:180.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A stirred, homogeneous mixture of finely powdered, compound 27 (17.0 g, 0.10 mol), aluminium chloride (29.4 g, 0.22 mol) and sodium chloride (7.1 g, 0.12 mol) was heated to 180° C. over 25 min and then at 180° C. for 1 h (glc and tlc analyses both revealed a complete reaction). Ice-water was added, and the product was extracted into ether (twice). The combined ethereal extracts were washed with water, and the product was extracted into 10% sodium hydroxide (twice) and the combined basic extracts were acidified with 36% hydrochloric acid. The product was extracted into ether (twice), and the combined ethereal extracts were washed with water and dried (MgSO4). The solvent was removed in vacuo to give a fawn solid. a complete reaction) the product was extracted into ether (twice) The combined ethereal extracts were washed with water the product was extracted into 10% sodium hydroxide (twice) and the combined basic extracts The product was extracted into ether (twice), and the combined ethereal extracts were washed with water dried (MgSO4) The solvent was removed in vacuo to give a fawn solid
来源 ID: ord-2f4bdb0a3888460ea89a01d4ed7a2a69反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e641ce8c83314945be60c04c47df8740PubChem References
以下资料来自该化合物的公开数据库参考记录。
