反应 #4056849
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-2f877b90652942a2be065831006a689e暂无可渲染的结构数据
CC(C)(CO)NC(=O)C1=C(C=C(C=C1F)F)F中间体产品
2,4,6-trifluoro-N-(1-hydroxy-2-methylpropan-2-yl)benzamide
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 | 2,4,6-三氟-N-(1-羟基-2-甲基丙-2-基)苯甲酰胺 |
|---|---|
| English name | 2,4,6-trifluoro-N-(1-hydroxy-2-methylpropan-2-yl)benzamide |
| IUPAC 名称 | — |
| CAS号 | 1360056-26-3 |
| 数据库编号 | 65100569 |
| 分子式 | — |
| 分子量 | — |
产品信息
2,4,6-三氟-N-(1-羟基-2-甲基丙-2-基)苯甲酰胺(CAS 1360056-26-3)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 65100569
安全提示
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合成路线数据
5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2f877b90652942a2be065831006a689e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2,4,6-trifluoro-N-(2-hydroxy-1,1-dimethyl-ethyl)-benzamide (43.8 g, 177.1 mmol) in dry dichloromethane (400 mL) was added thionyl chloride (58.9 ml, 415 mmol) via slow drop-wise addition over 25 minutes (reaction flask was immersed in an ice bath part way through the addition to control the temperature). After complete addition the material was stirred at ambient temperature over night. The volume was reduced to 30% by concentration under vacuum. To that was added ether (200 ml) and a solid precipitate (39.94 g off-white solid) was collected by filtration. The ether filtrate was set aside and the solid material was taken up in water (120 ml) and treated with an aqueous solution of sodium hydroxide (2N, 55 ml). Ethyl acetate (120 ml) was added and the mixture was transferred to a separatory funnel and shaken. The organic phase was collected and washed with an equal volume of water. The ethyl acetate phase was collected and the aqueous phases were back extracted with ethyl acetate (2×100 ml). The combined organic phases were dried (magnesium sulfate), filtered and concentrated in vacuo to provide the desired as a pure off-white solid (33.98 g). (M+H)+=230 m/e. via slow drop-wise addition over 25 minutes ( reaction flask was immersed in an ice bath part way through the addition After complete addition the material The volume was reduced to 30% by concentration under vacuum To that was added ether (200 ml) a solid precipitate (39.94 g off-white solid) was collected by filtration treated with an aqueous solution of sodium hydroxide (2N, 55 ml) Ethyl acetate (120 ml) was added the mixture was transferred to a separatory funnel shaken The organic phase was collected washed with an equal volume of water The ethyl acetate phase was collected the aqueous phases were back extracted with ethyl acetate (2×100 ml) The combined organic phases were dried (magnesium sulfate) filtered concentrated in vacuo to provide the
来源 ID: ord-0c56728d428c49f0ab48cb0db478b6fc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2f877b90652942a2be065831006a689e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2,4,6-trifluoro-N-(2-hydroxy-1,1-dimethyl-ethyl)-benzamide (43.8 g, 177.1 mmol) in dry dichloromethane (400 mL) was added thionyl chloride (58.9 ml, 415 mmol) via slow drop-wise addition over 25 minutes (reaction flask was immersed in an ice bath part way through the addition to control the temperature). After complete addition the material was stirred at ambient temperature over night. The volume was reduced to 30% by concentration under vacuum. To that was added ether (200 ml) and a solid precipitate (39.94 g off-white solid) was collected by filtration. The ether filtrate was set aside and the solid material was taken up in water (120 ml) and treated with an aqueous solution of sodium hydroxide (2N, 55 ml). Ethyl acetate (120 ml) was added and the mixture was transferred to a separatory funnel and shaken. The organic phase was collected and washed with an equal volume of water. The ethyl acetate phase was collected and the aqueous phases were back extracted with ethyl acetate (2×100 ml). The combined organic phases were dried (magnesium sulfate), filtered and concentrated in vacuo to provide the desired as a pure off-white solid (33.98 g). (M+H)+=230 m/e. via slow drop-wise addition over 25 minutes ( reaction flask was immersed in an ice bath part way through the addition After complete addition the material The volume was reduced to 30% by concentration under vacuum To that was added ether (200 ml) a solid precipitate (39.94 g off-white solid) was collected by filtration treated with an aqueous solution of sodium hydroxide (2N, 55 ml) Ethyl acetate (120 ml) was added the mixture was transferred to a separatory funnel shaken The organic phase was collected washed with an equal volume of water The ethyl acetate phase was collected the aqueous phases were back extracted with ethyl acetate (2×100 ml) The combined organic phases were dried (magnesium sulfate) filtered concentrated in vacuo to provide the
来源 ID: ord-c6c04292a93941549ca3c793a74ec182反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2,4,6-trifluoro-N-(2-hydroxy-1,1-dimethyl-ethyl)-benzamide (43.8 g, 177.1 mmol) in dry dichloromethane (400 mL) was added thionyl chloride (58.9 ml, 415 mmol) via slow drop-wise addition over 25 minutes (reaction flask was immersed in an ice bath part way through the addition to control the temperature). After complete addition the material was stirred at ambient temperature over night. The volume was reduced to 30% by concentration under vacuum. To that was added ether (200 ml) and a solid precipitate (39.94 g off-white solid) was collected by filtration. The ether filtrate was set aside and the solid material was taken up in water (120 ml) and treated with an aqueous solution of sodium hydroxide (2N, 55 ml). Ethyl acetate (120 ml) was added and the mixture was transferred to a separatory funnel and shaken. The organic phase was collected and washed with an equal volume of water. The ethyl acetate phase was collected and the aqueous phases were back extracted with ethyl acetate (2×100 ml). The combined organic phases were dried (magnesium sulfate), filtered and concentrated in vacuo to provide the desired as a pure off-white solid (33.98 g). (M+H)+=230 m/e. via slow drop-wise addition over 25 minutes ( reaction flask was immersed in an ice bath part way through the addition After complete addition the material The volume was reduced to 30% by concentration under vacuum To that was added ether (200 ml) a solid precipitate (39.94 g off-white solid) was collected by filtration treated with an aqueous solution of sodium hydroxide (2N, 55 ml) Ethyl acetate (120 ml) was added the mixture was transferred to a separatory funnel shaken The organic phase was collected washed with an equal volume of water The ethyl acetate phase was collected the aqueous phases were back extracted with ethyl acetate (2×100 ml) The combined organic phases were dried (magnesium sulfate) filtered concentrated in vacuo to provide the
来源 ID: ord-0c56728d428c49f0ab48cb0db478b6fcPubChem References
以下资料来自该化合物的公开数据库参考记录。
