反应 #4175107
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-af0d6cd93abf4d79ae062cd6b8557385暂无可渲染的结构数据
CC(C)(C)C1=C(C=C(C=C1)O)F产品信息
4-tert-butyl-3-fluorophenol(CAS 886842-69-9)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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合成路线数据
10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-af0d6cd93abf4d79ae062cd6b8557385反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-338a89d5fc4a4f77a0bdb564866fc6f2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-699eaa0db0104be5b66a75fcf0680f4c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-338a89d5fc4a4f77a0bdb564866fc6f2反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Zirconiumtetrachloride (11.7 g, 50 mmol) in DCM (130 ml), tert-butylmethylether (4.44 g, 50 mmol), and 3-fluorophenol (5.6 g, 50 mmol) were mixed at room temperature and the reaction mixture was stirred for 2 hours at 50° C. The reaction was quenched with water and the whole was extracted with ethylacetate and dried over magnesium sulfate. After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography, eluting with gradually from hexane only to hexane/ethylacetate (9:1), to afford 4.25 g (51% yield) of the title compound as white solids. The reaction was quenched with water the whole was extracted with ethylacetate dried over magnesium sulfate After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography eluting with gradually from hexane only to hexane/ethylacetate (9:1)
来源 ID: ord-bba104deea6046ed9c135fafca856a3d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-699eaa0db0104be5b66a75fcf0680f4c反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Zirconiumtetrachloride (11.7 g, 50 mmol) in DCM (130 ml), tert-butylmethylether (4.44 g, 50 mmol), and 3-fluorophenol (5.6 g, 50 mmol) were mixed at room temperature and the reaction mixture was stirred for 2 hours at 50° C. The reaction was quenched with water and the whole was extracted with ethylacetate and dried over magnesium sulfate. After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography, eluting with gradually from hexane only to hexane/ethylacetate (9:1), to afford 4.25 g (51% yield) of the title compound as white solids. The reaction was quenched with water the whole was extracted with ethylacetate dried over magnesium sulfate After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography eluting with gradually from hexane only to hexane/ethylacetate (9:1)
来源 ID: ord-d1fc3123908a41b7b341037b6214df73反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Sixty % sodium hydride (128 mg, 3.2 mmol), 4-tert-butyl-3-fluorophenol (450 mg, 2.7 mmol), tert-butyl bromoacetate (632 mg, 3.2 mmol) were treated in the same procedure described in Example 3(b) to furnish 634 mg (82% yield) of the title compound as a white solid.
来源 ID: ord-58454812816f4f95a1c332263622964d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of zirconium tetrachloride (1.2 g, 5 mmol) in methylene dichloride (15 ml), methyl tert-butyl ether (0.44 g, 5 mmol), 3-fluorophenol (0.56 g, 5 mmol) were treated in the same procedure described in Example 3(a) to furnish 458 mg (55% yield) of the title compound as a white solid. were treated in the same procedure
来源 ID: ord-ff8dd3fefc0141a19c0e37b27d4aa1e1反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Zirconiumtetrachloride (11.7 g, 50 mmol) in DCM (130 ml), tert-butylmethylether (4.44 g, 50 mmol), and 3-fluorophenol (5.6 g, 50 mmol) were mixed at room temperature and the reaction mixture was stirred for 2 hours at 50° C. The reaction was quenched with water and the whole was extracted with ethylacetate and dried over magnesium sulfate. After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography, eluting with gradually from hexane only to hexane/ethylacetate (9:1), to afford 4.25 g (51% yield) of the title compound as white solids. The reaction was quenched with water the whole was extracted with ethylacetate dried over magnesium sulfate After filtration, evaporation gave a crude residue, which was purified by silica gel column chromatography eluting with gradually from hexane only to hexane/ethylacetate (9:1)
来源 ID: ord-bba104deea6046ed9c135fafca856a3dPubChem References
以下资料来自该化合物的公开数据库参考记录。
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