反应 #3861000
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-34cf3d5df4fd4f3ca52432afe92a46c3暂无可渲染的结构数据
CC(=O)CCO[Si](C)(C)C(C)(C)C中间体产品
4-[tert-butyl(dimethyl)silyl]oxybutan-2-one
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 | 4-[tert-butyl(dimethyl)silyl]oxybutan-2-one |
|---|---|
| English name | 4-[tert-butyl(dimethyl)silyl]oxybutan-2-one |
| IUPAC 名称 | — |
| CAS号 | 120591-36-8 |
| 数据库编号 | 11030898 |
| 分子式 | — |
| 分子量 | — |
产品信息
4-[tert-butyl(dimethyl)silyl]oxybutan-2-one(CAS 120591-36-8)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 11030898
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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
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-34cf3d5df4fd4f3ca52432afe92a46c3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product of Example 457A (2.0 g, 9.88 mmol) in anhydrous THF (50ml) under at 0 C under nitrogen was reacted with phenylmagnesium bromide as a 3.0M solution in ether (5.0 ml, 15 mmol) dropwise via syringe then stirred for one hour. The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride and the reaction was partitioned with ether and water. The combined organics were dried over magnesium sulfate and concentrated in vacuo to give the desired compound as a clear oil (2.71 g, quantitative). The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride the reaction was partitioned with ether and water The combined organics were dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-e69d2afde6594a77b31f8e8ce71820a4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product of Example 457A (2.0 g, 9.88 mmol) in anhydrous THF (50ml) under at 0 C under nitrogen was reacted with phenylmagnesium bromide as a 3.0M solution in ether (5.0 ml, 15 mmol) dropwise via syringe then stirred for one hour. The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride and the reaction was partitioned with ether and water. The combined organics were dried over magnesium sulfate and concentrated in vacuo to give the desired compound as a clear oil (2.71 g, quantitative). The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride the reaction was partitioned with ether and water The combined organics were dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-e69d2afde6594a77b31f8e8ce71820a4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Hydroxybutan-2-one (1.0 g, 11.35 mmol), imidazole (1.16 g, 17 mmol) in DMF (15 ml) was reacted with tert-butyldimethylsilyl chloride (1.7 g, 11.35 mmol) for three hours at room temperature. The reaction was partitioned with ether and water. The aqueous phase was extracted several times with ether. The combined organics were washed several times with water then dried over magnesium sulfate and concentrated in vacuo to give the title compound as a clear oil (2.16 g, 94%). The reaction was partitioned with ether and water The aqueous phase was extracted several times with ether The combined organics were washed several times with water then dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-e1427edce61d4dd1a12480b94ce9e50a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The product of Example 457A (2.0 g, 9.88 mmol) in anhydrous THF (50ml) under at 0 C under nitrogen was reacted with phenylmagnesium bromide as a 3.0M solution in ether (5.0 ml, 15 mmol) dropwise via syringe then stirred for one hour. The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride and the reaction was partitioned with ether and water. The combined organics were dried over magnesium sulfate and concentrated in vacuo to give the desired compound as a clear oil (2.71 g, quantitative). The reaction was quenched by the drop wise addition of a saturated solution of ammonium chloride the reaction was partitioned with ether and water The combined organics were dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-e69d2afde6594a77b31f8e8ce71820a4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Hydroxybutan-2-one (1.0 g, 11.35 mmol), imidazole (1.16 g, 17 mmol) in DMF (15 ml) was reacted with tert-butyldimethylsilyl chloride (1.7 g, 11.35 mmol) for three hours at room temperature. The reaction was partitioned with ether and water. The aqueous phase was extracted several times with ether. The combined organics were washed several times with water then dried over magnesium sulfate and concentrated in vacuo to give the title compound as a clear oil (2.16 g, 94%). The reaction was partitioned with ether and water The aqueous phase was extracted several times with ether The combined organics were washed several times with water then dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-e1427edce61d4dd1a12480b94ce9e50aPubChem References
以下资料来自该化合物的公开数据库参考记录。
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