反应 #4042665
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-702c8324416f4429a047081a6b2fc5f1暂无可渲染的结构数据
C1C(OC2=CC=CC=C2O1)CCO中间体产品
2-(2,3-dihydro-1,4-benzodioxin-3-yl)ethanol
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 | 2-(2,3-二氢苯并[B][1,4]二噁英-2-基)乙烷-1-醇 |
|---|---|
| English name | 2-(2,3-dihydro-1,4-benzodioxin-3-yl)ethanol |
| IUPAC 名称 | — |
| CAS号 | 62590-71-0 |
| 数据库编号 | 98334 |
| 分子式 | — |
| 分子量 | — |
产品信息
2-(2,3-二氢苯并[B][1,4]二噁英-2-基)乙烷-1-醇(CAS 62590-71-0)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 98334
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
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-702c8324416f4429a047081a6b2fc5f1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-56832b1c966244e99bfd53998192219b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-01dca1ce29844906a54cc5e6db0eefda反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-723f97a22136416a9892b97c65df18a5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-bc4cb421e31542ff9a53663627153c1b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-bc4cb421e31542ff9a53663627153c1b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-f10d21305eff4dd8a19eb31a5606586a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-f10d21305eff4dd8a19eb31a5606586a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 7.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-8ff1333e6fec46a391dca6448a604e97反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 7.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-8ff1333e6fec46a391dca6448a604e97反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-a6dd5f8a112d4c4797b2c829879165b6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the compound 2-hydroxyethyl-1,4-benzodioxan (11.96 g) in dichloromethane (450 ml) was added triethylamine (0.12 mol, 10 ml). Mesylchloride (9.2 g) was then added dropwise and the reaction mixture was stirred for one hour at room temperature. After completion of the reaction, the solution was washed with water, brine, and concentrated to an oil, which was purified by chromatography on silica gel to yield 2-mesyloxyethyl-1,4-benzodioxan, 17.08 g. After completion of the reaction the solution was washed with water, brine concentrated to an oil, which was purified by chromatography on silica gel
来源 ID: ord-14a48f44943543eebf33d2b2fa5ac8f3PubChem References
以下资料来自该化合物的公开数据库参考记录。
