反应 #4065129
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-7fd1fb553c6a416181061c126a424cf1暂无可渲染的结构数据
CC1(C(O1)C(=O)OC)C2=CC=CC=C2中间体产品
methyl 3-methyl-3-phenyloxirane-2-carboxylate
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 | Methyl β-methyl-β-phenylglycidate |
|---|---|
| English name | methyl 3-methyl-3-phenyloxirane-2-carboxylate |
| IUPAC 名称 | — |
| CAS号 | 5441-04-3 |
| 数据库编号 | 228011 |
| 分子式 | — |
| 分子量 | — |
产品信息
Methyl β-methyl-β-phenylglycidate(CAS 5441-04-3)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 228011
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-7fd1fb553c6a416181061c126a424cf1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-eed76475c00f456ca742fb9e8a0e6552反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 51.9 g (0.3 mol) of 4-bromophenol and 19.2 g (0.1 mol) of methyl 3-phenyl-2,3-epoxybutyrate are stirred at 100° C. for 8 hours and at room temperature for 12 hour. After removal of the excess phenol by distillation, the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1) to result in 7.2 g of a white solid. After removal of the excess phenol by distillation the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1)
来源 ID: ord-d9675b544e26491989ee50b08f760dbe反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 9.6 g (50 mmol) of methyl 3-phenyl-2,3-epoxybutyrate are dissolved in 150 ml of benzyl alcohol, and 0.5 ml of concentrated sulfuric acid is added. The mixture is stirred at 50° C. for 6 hours and allowed to cool to room temperature. After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum, and the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate. After removal of the solvent by distillation, 6.5 g of a colorless oil remain. to cool to room temperature After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate After removal of the solvent by distillation, 6.5 g of a colorless oil
来源 ID: ord-ec22ef5365b144248f249b920c5151a0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 51.9 g (0.3 mol) of 4-bromophenol and 19.2 g (0.1 mol) of methyl 3-phenyl-2,3-epoxybutyrate are stirred at 100° C. for 8 h and at room temperature for 12 h. After removal of the excess phenol by distillation, the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1) to result in 7.2 g of a white solid. After removal of the excess phenol by distillation the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1)
来源 ID: ord-14124aa0e8a44e7292a3a62925bde09f反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 9.6 g (50 mmol) of methyl 3-phenyl-2,3-epoxybutyrate are dissolved in 150 ml of benzyl alcohol, and 0.5 ml of concentrated sulfuric acid is added. The mixture is stirred at 50° C. for 6 hours and allowed to cool to room temperature. After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum, and the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate. After removal of the solvent by distillation, 6.5 g of a colorless oil remain. to cool to room temperature After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate After removal of the solvent by distillation, 6.5 g of a colorless oil
来源 ID: ord-afe9f54ad3f14695a2cdf9ae4e5dd264反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 51.9 g (0.3 mol) of 4-bromophenol and 19.2 g (0.1 mol) of methyl 3-phenyl-2,3-epoxybutyrate are stirred at 100° C. for 8 hours and at room temperature for 12 hour. After removal of the excess phenol by distillation, the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1) to result in 7.2 g of a white solid. After removal of the excess phenol by distillation the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1)
来源 ID: ord-d9675b544e26491989ee50b08f760dbe反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 9.6 g (50 mmol) of methyl 3-phenyl-2,3-epoxybutyrate are dissolved in 150 ml of benzyl alcohol, and 0.5 ml of concentrated sulfuric acid is added. The mixture is stirred at 50° C. for 6 hours and allowed to cool to room temperature. After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum, and the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate. After removal of the solvent by distillation, 6.5 g of a colorless oil remain. to cool to room temperature After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate After removal of the solvent by distillation, 6.5 g of a colorless oil
来源 ID: ord-ec22ef5365b144248f249b920c5151a0反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 9.6 g (50 mmol) of methyl 3-phenyl-2,3-epoxybutyrate are dissolved in 150 ml of benzyl alcohol, and 0.5 ml of concentrated sulfuric acid is added. The mixture is stirred at 50° C. for 6 hours and allowed to cool to room temperature. After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum, and the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate. After removal of the solvent by distillation, 6.5 g of a colorless oil remain. to cool to room temperature After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate After removal of the solvent by distillation, 6.5 g of a colorless oil
来源 ID: ord-ec22ef5365b144248f249b920c5151a0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 51.9 g (0.3 mol) of 4-bromophenol and 19.2 g (0.1 mol) of methyl 3-phenyl-2,3-epoxybutyrate are stirred at 100° C. for 8 h and at room temperature for 12 h. After removal of the excess phenol by distillation, the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1) to result in 7.2 g of a white solid. After removal of the excess phenol by distillation the residue is purified by flash chromatography (silica gel, n-hexane/ethyl acetate 9:1)
来源 ID: ord-14124aa0e8a44e7292a3a62925bde09f反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 9.6 g (50 mmol) of methyl 3-phenyl-2,3-epoxybutyrate are dissolved in 150 ml of benzyl alcohol, and 0.5 ml of concentrated sulfuric acid is added. The mixture is stirred at 50° C. for 6 hours and allowed to cool to room temperature. After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum, and the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate. After removal of the solvent by distillation, 6.5 g of a colorless oil remain. to cool to room temperature After neutralization with sodium bicarbonate solution, the excess benzyl alcohol is removed by distillation under high vacuum the residue is purified by flash chromatography on silica gel with 9:1 n-hexane/ethyl acetate After removal of the solvent by distillation, 6.5 g of a colorless oil
来源 ID: ord-afe9f54ad3f14695a2cdf9ae4e5dd264反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7fd1fb553c6a416181061c126a424cf1PubChem References
以下资料来自该化合物的公开数据库参考记录。
