反应 #4109246
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d2b96ed3b34d4172b4cff94abc8559b6暂无可渲染的结构数据
COC1=C(C=CC(=C1)C=C2C(=O)NC(=O)N2)O中间体产品
5-[(4-hydroxy-3-methoxyphenyl)methylidene]imidazolidine-2,4-dione
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 5-[(4-羟基-3-甲氧基苯基)亚甲基]咪唑烷-2,4-二酮 |
|---|---|
| English name | 5-[(4-hydroxy-3-methoxyphenyl)methylidene]imidazolidine-2,4-dione |
| IUPAC 名称 | — |
| CAS号 | 52036-16-5 |
| 数据库编号 | 291123 |
| 分子式 | — |
| 分子量 | — |
产品信息
5-[(4-羟基-3-甲氧基苯基)亚甲基]咪唑烷-2,4-二酮(CAS 52036-16-5)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 291123
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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d2b96ed3b34d4172b4cff94abc8559b6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-hydroxy-3-methoxybenzaldehyde (4.6 g, 30 mmoles), hydantoin (3.0 g, 30 mmoles), β-alanine (1.4 g, 16 mmoles), and acetic acid (40 ml) is stirred under an inert atmosphere and heated to reflux. After 4 hours the mixture is stirred into water (350 ml) and the precipitate is filtered off, rinsed successively with water (3×), ethanol (2×), and ether (2×), and dried. Recrystallization from methanol afforded the pure product (3.0 g), mp 272°-273° C. heated to reflux the precipitate is filtered off rinsed successively with water (3×), ethanol (2×), and ether (2×) dried Recrystallization from methanol
来源 ID: ord-74ffa3a6e3d54efea25b1f3ed264a027反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-hydroxy-3-methoxybenzaldehyde (4.6 g, 30 mmoles), hydantoin (3.0 g, 30 mmoles), β-alanine (1.4 g, 16 mmoles), and acetic acid (40 ml) is stirred under an inert atmosphere and heated to reflux. After 4 hours the mixture is stirred into water (350 ml) and the precipitate is filtered off, rinsed successively with water (3×), ethanol (2×), and ether (2×), and dried. Recrystallization from methanol afforded the pure product (3.0 g), mp 272°-273° C. heated to reflux the precipitate is filtered off rinsed successively with water (3×), ethanol (2×), and ether (2×) dried Recrystallization from methanol
来源 ID: ord-74ffa3a6e3d54efea25b1f3ed264a027反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: condensing vanillin and hydantoin by heating together in admixture with diethanolamine to produce 5-vanillylidenehydantoin, and
来源 ID: ord-19de35e3b8dd432b9068efdf1294c89b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Vanillin (3.04 g.) and hydantoin (2.0 g.) in water (20 ml were heated on the steam-bath for a few minutes until dissolution occurred. Ethanolamine (0174 g.) was then added and the solution heated at 85°-90° (bath temperature) for 4.5 hours. The solution deposited crystals and solidified within 0.5 hours. Concentrated HCl (5 ml) was added, the mixture was refrigerated overnight (18 hours), filtered, water washed and dried. The title compound was obtained as a yellow solid (4.18 g; 93%), m.p. 266°-271° decomp. the solution heated at 85°-90° (bath temperature) for 4.5 hours the mixture was refrigerated overnight (18 hours), filtered water washed dried
来源 ID: ord-525864cc2b2749e795906a9f6e30ff42反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Vanillin (3.04 g.) and hydantoin (2.0 g.) in water (20 ml were heated on the steam-bath for a few minutes until dissolution occurred. Ethanolamine (0174 g.) was then added and the solution heated at 85°-90° (bath temperature) for 4.5 hours. The solution deposited crystals and solidified within 0.5 hours. Concentrated HCl (5 ml) was added, the mixture was refrigerated overnight (18 hours), filtered, water washed and dried. The title compound was obtained as a yellow solid (4.18 g; 93%), m.p. 266°-271° decomp. the solution heated at 85°-90° (bath temperature) for 4.5 hours the mixture was refrigerated overnight (18 hours), filtered water washed dried
来源 ID: ord-525864cc2b2749e795906a9f6e30ff42反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Vanillin (3.04 g.) and hydantoin (2.0 g.) in water (20 ml) were heated on the steam-bath for a few minutes until dissolution occurred. Ethanolamine (0174 g.) was then added and the solution heated at 85°-90° (bath temperature) for 4.5 hours. The solution deposited crystals and solidified within 0.5 hours. Concentrated HCl (5 ml) was added, the mixture was refrigerated overnight (18 hours), filtered, water washed and dried. The title compound was obtained as a yellow solid (4.18 g; 93%), m.p. 266°-271° decomp. the solution heated at 85°-90° (bath temperature) for 4.5 hours the mixture was refrigerated overnight (18 hours), filtered water washed dried
来源 ID: ord-0bf033c6646e4585962f719b2b38f4d7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Vanillin (3.04 g.) and hydantoin (2.0 g.) in water (20 ml were heated on the steam-bath for a few minutes until dissolution occurred. Ethanolamine (0174 g.) was then added and the solution heated at 85°-90° (bath temperature) for 4.5 hours. The solution deposited crystals and solidified within 0.5 hours. Concentrated HCl (5 ml) was added, the mixture was refrigerated overnight (18 hours), filtered, water washed and dried. The title compound was obtained as a yellow solid (4.18 g; 93%), m.p. 266°-271° decomp. the solution heated at 85°-90° (bath temperature) for 4.5 hours the mixture was refrigerated overnight (18 hours), filtered water washed dried
来源 ID: ord-6286c83b5cd54305a53e23f49fee60cb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Vanillin (3.04 g.) and hydantoin (2.0 g.) in water (20 ml were heated on the steam-bath for a few minutes until dissolution occurred. Ethanolamine (0174 g.) was then added and the solution heated at 85°-90° (bath temperature) for 4.5 hours. The solution deposited crystals and solidified within 0.5 hours. Concentrated HCl (5 ml) was added, the mixture was refrigerated overnight (18 hours), filtered, water washed and dried. The title compound was obtained as a yellow solid (4.18 g; 93%), m.p. 266°-271° decomp. the solution heated at 85°-90° (bath temperature) for 4.5 hours the mixture was refrigerated overnight (18 hours), filtered water washed dried
来源 ID: ord-6286c83b5cd54305a53e23f49fee60cb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-hydroxy-3-methoxybenzaldehyde (4.6 g, 30 mmoles), hydantoin (3.0 g, 30 mmoles), β-alanine (1.4 g, 16 mmoles), and acetic acid (40 ml) is stirred under an inert atmosphere and heated to reflux. After 4 hours the mixture is stirred into water (350 ml) and the precipitate is filtered off, rinsed successively with water (3×), ethanol (2×), and ether (2×), and dried. Recrystallization from methanol afforded the pure product (3.0 g), mp 272°-273° C. heated to reflux the precipitate is filtered off rinsed successively with water (3×), ethanol (2×), and ether (2×) dried Recrystallization from methanol
来源 ID: ord-74ffa3a6e3d54efea25b1f3ed264a027反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-hydroxy-3-methoxybenzaldehyde (4.6 g, 30 mmoles), hydantoin (3.0 g, 30 mmoles), β-alanine (1.4 g, 16 mmoles), and acetic acid (40 ml) is stirred under an inert atmosphere and heated to reflux. After 4 hours the mixture is stirred into water (350 ml) and the precipitate is filtered off, rinsed successively with water (3X), ethanol (2X), and ether (2X), and dried. Recrystallization from methanol afforded the pure product (3.0 g), mp 272°-273° C. heated to reflux the precipitate is filtered off rinsed successively with water (3X), ethanol (2X), and ether (2X) dried Recrystallization from methanol
来源 ID: ord-1b54489de7de41f3a8ce65b641fabe5d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d2b96ed3b34d4172b4cff94abc8559b6PubChem References
以下资料来自该化合物的公开数据库参考记录。
