反应 #4174029
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-62087cea1449421f825fefc114888ca5暂无可渲染的结构数据
C1=CC(=CC(=C1)C(F)(F)F)CCl产品信息
1-氯甲基-3-三氟甲基苯(CAS 705-29-3)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。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-62087cea1449421f825fefc114888ca5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ac02e7b07ba74f2aae37df04c8e11fbb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-42511748e80e4acb9ed590d81ae4b738反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ec80722e104d4f4e879e0d9d50af5dcd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-71f27d4473a041859ccba184b009f08c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-eb10d9aee72c4c93afb9c88b85f60cee反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-df0516b6cfc4444a85548ec9d1d990c4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d14415c574554e488ecd70443e12fa1e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fc404e8dfd0a4811bfbedf73d892ea2d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b224611d9d7947c2a19b7a72f890c25a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 50 ml DMF were added 11-(piperidin-4-yl)-5H,11H-pyrrolo[2,1-c][1,4]benzoxazepine (6.0 g, 0.022 mole), 3-trifluoromethylbenzyl chloride (5.0 g, 0.026 mole), milled K2CO3 (10 g, 0.07 mole) and KI (0.01 g).
来源 ID: ord-adfb9a126aaa429f9947c6e466867613反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A reaction vessel was charged with 50 ml of dimethylformamide, 2.6 g (18.8 mmol) of potassium carbonate, and 5.36 g (28 mmol) of m-trifluoromethyl benzyl chloride. With this mixture stirred at ambient temperature under a nitrogen atmosphere, there was added 4.03 g (17 mmol) of 2-[(1,1-dimethylethyl)amino]-4-trifluoromethyl-5-oxazolecarboxylic acid (prepared by Example 26). The reaction mixture was stirred at ambient temperature for 36 hours. Then, the mixture was added to water and extracted four times with ethyl ether. The ether extracts were washed with large amounts of water, then dried over magnesium sulfate, and concentrated under reduced pressure to yield 11.25 g of a yellow oily solid material. This solid material was dissolved in ethyl ether, washed with large amounts of water, dried over magnesium sulfate, and concentrated under reduced pressure to yield 10.8 g of a gold viscous oil. Then, 5.0 g of this oil was subjected to Kugelrohr distillation (83°-85° C. @ 0.5 mm Hg) to yield 1.38 g of a gold viscous oil which upon standing overnight formed an oily solid product identified in Table I. The reaction mixture was stirred at ambient temperature for 36 hours extracted four times with ethyl ether The ether extracts were washed with large amounts of water dried over magnesium sulfate concentrated under reduced pressure
来源 ID: ord-f41480956bf54120be82fca5e5f77391PubChem References
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