反応 #4175107
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-af0d6cd93abf4d79ae062cd6b8557385表示可能な構造データがありません
CC(C)(C)C1=C(C=C(C=C1)O)F製品情報
4-tert-butyl-3-fluorophenol (CAS 886842-69-9) 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 20583424
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
10 反応 · 10 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-af0d6cd93abf4d79ae062cd6b8557385反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-338a89d5fc4a4f77a0bdb564866fc6f2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-699eaa0db0104be5b66a75fcf0680f4c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-338a89d5fc4a4f77a0bdb564866fc6f2反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-bba104deea6046ed9c135fafca856a3d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-699eaa0db0104be5b66a75fcf0680f4c反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-d1fc3123908a41b7b341037b6214df73反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-58454812816f4f95a1c332263622964d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-ff8dd3fefc0141a19c0e37b27d4aa1e1反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-bba104deea6046ed9c135fafca856a3dPubChem References
化合物の公開データベース記録に掲載された情報源です。
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