反応 #4133829
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-e8ea2283e47e4e328bf6a880a9bac9e1表示可能な構造データがありません
COC1=CC=CC=C1I製品情報
1-iodo-2-methoxybenzene (CAS 529-28-2) 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 68257
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-e8ea2283e47e4e328bf6a880a9bac9e1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9e7fdca9a73847468404bde8f0d637f4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a4abef4432994ad7a796e6dca6817b59反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-7c0c641ed4a6477ebfd4fd4fae808f46反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b17eb868bf7c4a69bba998727b3f9033反応条件: temp:200.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Iodoanisole (1.30 mL, 0.01 mol), 2-hydroxypyridine (0.95 g, 0.01 mol), anhydrous K2CO3 (2.76 g, 0.02 mol) and copper powder (0.0636 g, 0.001 mol) were combined and heated at 200° C. for 2 hr. The reaction mixture was cooled, EtOAc added, and filtered. The filtrate was washed with H2O, aqueous saturated NaHCO3 solution, brine, and dried (Na2SO4). Filtration and concentration gave the title compound after chromatography (silica gel, 2% CH3OH, CH2Cl2). The reaction mixture was cooled filtered The filtrate was washed with H2O, aqueous saturated NaHCO3 solution, brine dried (Na2SO4) Filtration and concentration
ソース ID: ord-4c3a55ba796041aab00b78a70ae21ba3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e8ea2283e47e4e328bf6a880a9bac9e1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-27cf2b481e8f4ea0b21c07132f95f6be反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a stirred, cold (-78° C.) solution of 2-iodoanisole (2.85 ml, 5.6 g) in 50 ml of tetrahydrofuran under nitrogen was added 10.0 ml of 2.5M n-butyl lithium in hexane. After 15 min. triisopropyl borate (3.38 ml, 4.7 g) was added and the reaction was allowed to come to and remain at room temperature for 1.5 hr. The mixture was poured into an excess of 2N hydrochloric acid and diethyl ether was added. The resulting mixture was stirred vigorously for 30 min. and the phases were separated. The ether layer was washed with aqueous sodium bisulfite until colorless and then with saturated sodium chloride solution and then dried over magnesium sulfate. Concentration of the ether layer gave the crude boronic acid which crystallized from ether to give the title product. was added the phases were separated The ether layer was washed with aqueous sodium bisulfite until colorless and then with saturated sodium chloride solution dried over magnesium sulfate Concentration of the ether layer gave the crude boronic acid which crystallized from ether
ソース ID: ord-9648bcaa93904f84bff8f019a351e1c5PubChem 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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