反応 #4155794
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-5a96adacad9540e88e888d1cc7503869表示可能な構造データがありません
C1=CC=C(C=C1)COC(=O)CCCBr製品情報
benzyl 4-bromobutanoate (CAS 126430-46-4) 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 3832489
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-5a96adacad9540e88e888d1cc7503869反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-59e0108910f145b28d8483e8bae7d551反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5b084bc4834345b58addfb04668e1bc8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1c87a89b2d5c421c8837b6ff0e90cb02反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08cb776eaacb47b28b0646c14bd6247b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d7c1185aa74447399c13c047186dab73反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-daf466bf46cb4a9b8cf7a30e0c9a35f3反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4.7 g of 1,2,4-triazole and 9.5 g of potassium carbonate were added to a solution of 15 g of benzyl 4-bromobutyrate in 150 ml of acetonitrile. The mixture was refluxed by heating, for 1 hour. The reaction mixture was concentrated under reduced pressure. To the residue was added 30 ml of methylene chloride. The insolubles were collected by filtration and washed. The filtrate and the washings were combined and purified by silica gel column chromatography (eluant: methylene chloride/methanol=50/1) to obtain 11.6 g of benzyl 4-(1,2,4-triazol-1-yl)butyrate as a colorless oily substance. The mixture was refluxed by heating, for 1 hour The reaction mixture was concentrated under reduced pressure To the residue was added 30 ml of methylene chloride The insolubles were collected by filtration washed purified by silica gel column chromatography (eluant: methylene chloride/methanol=50/1)
ソース ID: ord-b58e6b6410494dc2a004a63ddfa11be4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5a96adacad9540e88e888d1cc7503869反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-59e0108910f145b28d8483e8bae7d551反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-59e0108910f145b28d8483e8bae7d551反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of benzyl 4-bromobutanoate (58.6 diethylamine (58.3 g) and dichloromethane (1000 ml) was stirred under reflux for 14 hours. The reaction mixture was washed with water and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel. The fractions eluted with ethyl acetate gave benzyl 4-(N,N-diethylamino)butanoate (33.8 g, 60%). under reflux for 14 hours The reaction mixture was washed with water dried over magnesium sulfate the solvent was evaporated under reduced pressure The fractions eluted with ethyl acetate
ソース ID: ord-5a0cea2b15534838b31d8da8b7eb66e2PubChem 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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