反应 #4040686
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-dc1d150b1fff4fd5bc9c3b420cad3ffd暂无可渲染的结构数据
CS(=O)(=O)C1=CC=C(C=C1)CC#N产品信息
4-(甲基磺酰基)苯乙腈(CAS 25025-07-4)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。
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7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-dc1d150b1fff4fd5bc9c3b420cad3ffd反应条件: temp:21.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of Quinoline 04 (5 g, 18 mmol), 4-methanesulfonylacetonitrile (3.5 g, 18 mmol) from Step 1 and piperidine (0.1 mL) in toluene (5 mL) was heated at 130° C. After 6 h, the mixture was cooled to 21° C. and purified by flash chromatography (eluting with ethylacetate/hexane, 1:1 to 75:25) to afforded the title compound. purified by flash chromatography (eluting with ethylacetate/hexane, 1:1 to 75:25)
来源 ID: ord-8451bab0a5a742e684ac51435d4e5a69反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-methanesulfonylbenzyl chloride (10 g, 49 mmol) in DMF (100 mL) was added HMPA (9.35 mL, 54 mmol) and KCN (3.5 g, 54 mmol). The resulting reaction mixture was stirred 18 h at 80° C., then diluted with water and ethyl acetate. The organic extracts were washed (NaHCO3, brine), dried (MgSO4), filtered and concentrated. Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75) provided the (4-methanesulfonyl-phenyl)-acetonitrile compound. The resulting reaction mixture The organic extracts were washed (NaHCO3, brine) dried (MgSO4) filtered concentrated Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75)
来源 ID: ord-aa32c99910224dc6b57ac9057e058132反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-methanesulfonylbenzyl chloride (10 g, 49 mmol) in DMF (100 mL) was added HMPA (9.35 mL, 54 mmol) and KCN (3.5 g, 54 mmol). The resulting reaction mixture was stirred 18 h at 80° C., then diluted with water and ethyl acetate. The organic extracts were washed (NaHCO3, brine), dried (MgSO4), filtered and concentrated. Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75) provided the (4-methanesulfonyl-phenyl)-acetonitrile compound. The resulting reaction mixture The organic extracts were washed (NaHCO3, brine) dried (MgSO4) filtered concentrated Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75)
来源 ID: ord-aa32c99910224dc6b57ac9057e058132反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-dc1d150b1fff4fd5bc9c3b420cad3ffd反应条件: temp:21.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of Quinoline 04 (5 g, 18 mmol), 4-methanesulfonylacetonitrile (3.5 g, 18 mmol) from Step 1 and piperidine (0.1 mL) in toluene (5 mL) was heated at 130° C. After 6 h, the mixture was cooled to 21° C. and purified by flash chromatography (eluting with ethylacetate/hexane, 1:1 to 75:25) to afforded the title compound. purified by flash chromatography (eluting with ethylacetate/hexane, 1:1 to 75:25)
来源 ID: ord-8451bab0a5a742e684ac51435d4e5a69反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-methanesulfonylbenzyl chloride (10 g, 49 mmol) in DMF (100 mL) was added HMPA (9.35 mL, 54 mmol) and KCN (3.5 g, 54 mmol). The resulting reaction mixture was stirred 18 h at 80° C., then diluted with water and ethyl acetate. The organic extracts were washed (NaHCO3, brine), dried (MgSO4), filtered and concentrated. Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75) provided the (4-methanesulfonyl-phenyl)-acetonitrile compound. The resulting reaction mixture The organic extracts were washed (NaHCO3, brine) dried (MgSO4) filtered concentrated Purification by flash chromatography (eluting with hexane/ethyl acetate, 1:1 to 25:75)
来源 ID: ord-aa32c99910224dc6b57ac9057e058132PubChem References
以下资料来自该化合物的公开数据库参考记录。
