反応 #4086953
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-96793f9fcc584dfda0813e03b1c3d606表示可能な構造データがありません
C1=CC(=C(C(=C1)O)C(=O)N)O製品情報
2,6-dihydroxybenzamide (CAS 3147-50-0) 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 76602
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-96793f9fcc584dfda0813e03b1c3d606反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-77dca147f7b040fa94903350b02c0755反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-6f3ffc5c3dae437286a22103a3ef822f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-6f3ffc5c3dae437286a22103a3ef822f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-47163b8fb6ae49a9b4394f743130485c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-47163b8fb6ae49a9b4394f743130485c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-2158019772d240b48c99ecea1fc7c2f3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-96793f9fcc584dfda0813e03b1c3d606反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-77dca147f7b040fa94903350b02c0755反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-2158019772d240b48c99ecea1fc7c2f3反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane in 300 ml of acetonitrile is stirred under reflux for 2-3 hours. The reaction mixture is filtered whilst still warm, the filtrate is evaporated and the residue is recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide with a melting point of 120°-121° is obtained. under reflux for 2-3 hours The reaction mixture is filtered whilst still warm the filtrate is evaporated the residue is recrystallised from a little methanol
ソース ID: ord-49770e2ac2594147b3c911489fde6c82反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 23.0 g of 2,6-dihydroxybenzamide, 20.7 g of potassium carbonate and 28.2 g of 1,2-dibromoethane is refluxed, whilst stirring, for 2-3 hours in 300 ml of acetonitrile. The reaction mixture is filtered whilst still warm, the filtrate concentrated by evaporation and the residue recrystallised from a little methanol. 6-(2-Bromoethoxy)salicylamide having a melting point of 120°-121° is obtained. is refluxed The reaction mixture is filtered whilst still warm the filtrate concentrated by evaporation the residue recrystallised from a little methanol
ソース ID: ord-2158019772d240b48c99ecea1fc7c2f3PubChem 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。
