反应 #4073678
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-0e9948c8419b4f5286715d7f4f9f55eb暂无可渲染的结构数据
CC(=CCCCCBr)C产品信息
7-溴-2-甲基庚-2-烯(CAS 58335-23-2)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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5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0e9948c8419b4f5286715d7f4f9f55eb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 11 g of 6-methyl-5-heptenyl tosylate in 100 ml of THF were added 10 ml of HMPA, 50 g of potassium bromide and 300 mg of 18-crown-6, and the resulting mixture was refluxed for 5 hours. After cooling, water was added, and the mixture was concentrated, the residue was extracted with pentane 3 times, the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine, dried and concentrated to give 8 g of an oily substance. This oily substance was distilled (bp 70° C./5 mm Hg) to yield 5.7 g of a pure bromide. the resulting mixture was refluxed for 5 hours After cooling the mixture was concentrated the residue was extracted with pentane 3 times the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine dried concentrated to give 8 g of an oily substance This oily substance was distilled (bp 70° C./5 mm Hg)
来源 ID: ord-215c7dc6a5fa4b3cb39fc1bbe6dddc3a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0e9948c8419b4f5286715d7f4f9f55eb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 11 g of 6-methyl-5-heptenyl tosylate in 100 ml of THF were added 10 ml of HMPA, 50 g of potassium bromide and 300 mg of 18-crown-6, and the resulting mixture was refluxed for 5 hours. After cooling, water was added, and the mixture was concentrated, the residue was extracted with pentane 3 times, the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine, dried and concentrated to give 8 g of an oily substance. This oily substance was distilled (bp 70° C./5 mm Hg) to yield 5.7 g of a pure bromide. the resulting mixture was refluxed for 5 hours After cooling the mixture was concentrated the residue was extracted with pentane 3 times the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine dried concentrated to give 8 g of an oily substance This oily substance was distilled (bp 70° C./5 mm Hg)
来源 ID: ord-c1258102ce01404095765d37d5a4f794反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 11 g of 6-methyl-5-heptenyl tosylate in 100 ml of THF were added 10 ml of HMPA, 50 g of potassium bromide and 300 mg of 18-crown-6, and the resulting mixture was refluxed for 5 hours. After cooling, water was added, and the mixture was concentrated, the residue was extracted with pentane 3 times, the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine, dried and concentrated to give 8 g of an oily substance. This oily substance was distilled (bp 70° C./5 mm Hg) to yield 5.7 g of a pure bromide. the resulting mixture was refluxed for 5 hours After cooling the mixture was concentrated the residue was extracted with pentane 3 times the combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate water and saturated brine dried concentrated to give 8 g of an oily substance This oily substance was distilled (bp 70° C./5 mm Hg)
来源 ID: ord-215c7dc6a5fa4b3cb39fc1bbe6dddc3aPubChem References
以下资料来自该化合物的公开数据库参考记录。
