反応 #4156464
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-13e4cecb6bd341b8a356e4baec51c648表示可能な構造データがありません
COC1=C(C=C(C=C1)C=O)Br製品情報
3-bromo-4-methoxybenzaldehyde (CAS 34841-06-0) 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 98662
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-13e4cecb6bd341b8a356e4baec51c648反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-245f051c2da141268272a791c93f65ba反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-baebe1012cbd45b1b90afcbc824fc9b3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f1a713eec8ac4aa0865c206ac42b8f64反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-80c7b93c4809414f8f16067d176585a1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5375cda7d76840fc9a8c04621d58533f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8479535501404375b6306d98c3810ced反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0688361ad893483bb4c607c010fdaf98反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-bb7e44b955084abf8b757247f9ef6cf4反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of sodium ethylate in ethanol (prepared from sodium (1.92 g; 83.70 mmol) and EtOH (40 mL)) was added dropwise to a cold (−10° C.) solution of 3-bromo-p-anisaldehyde (4 g; 18.60 mmol) and ethyl azidoacetate (ABCR, 27.80 ml; 46.50 mmol) in EtOH (60 mL). After the end of the addition, the reaction mixture was warmed up to 0° C. and stirred at RT for 5 hours. The heterogenous mixture was poured onto ice and stirred for 30 minutes. The solid was collected by filtration and dried under high vacuum. The solid was taken up in xylenes (60 mL) and heated to reflux for 3 hours. The solvent was evaporated and the residue was purified by silica column chromatography (c-Hexane/ethyl acetate, 80/20) to give the title compound as a pale yellow solid. 1H NMR (DMSO-d6) δ 11.87 (s, 1H), 7.89 (s, 1H), 7.05 (s, 1H), 6.98 (s, 1H), 4.31 (q, J=7 Hz, 2H), 3.85 (s, 3H), 1.32 (t, J=7 Hz, 3H). HPLC (Method A), Rt 4.28 min (Purity: 98.1%). LC/MS (Method B): 297.2 (M+H)+. After the end of the addition The heterogenous mixture was poured onto ice stirred for 30 minutes The solid was collected by filtration dried under high vacuum heated to reflux for 3 hours The solvent was evaporated the residue was purified by silica column chromatography (c-Hexane/ethyl acetate, 80/20)
ソース ID: ord-31cfe72e145c442c9af98cb8cdb4e709反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Addition of 3-bromo-4-methoxybenzaldehyde to acetonitrile gave 3-(3-bromo-4-methoxyphenyl)-3-hydroxypropanenitrile as a pale orange oil. Yield (10.32 g, 96%): 1H NMR (400 MHz, DMSO-d6) δ 7.58 (d, J=2.0 Hz, 1H), 7.35 (dd, J=8.8, 2.0 Hz, 1H), 7.07 (d, J=8.8 Hz, 1H), 5.93 (d, J=4.4 Hz, 1H), 4.85-4.81 (m, 1H). 3.81 (s, 3H), 2.86 (ABd, J=16.4, 4.8 Hz, 1H), 2.79 (ABd, J=16.8, 6.8 Hz, 1H).
ソース ID: ord-7fac66f00e2340bfb00ffcedc597dcc8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-13e4cecb6bd341b8a356e4baec51c648PubChem 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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