反应 #4133143
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-b5cb7f5567294fc5ad7fb1824458fa7f暂无可渲染的结构数据
C(CCCCCCBr)CCCCCO产品信息
12-溴十二烷-1-ol(CAS 3344-77-2)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-acb456d03a8847f18f67617bb9507ef0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2c3706e2eceb4af3b09a13a47517c648反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Na (800 mg, 34.8 mmol) was dissolved in 30 mL of dry MeOH. Under argon, p-methoxybenzylmercaptan (2.75 mL, 3.04 g, 19.7 mmol) was added to the methoxide solution. After a few minutes, 12-bromododecanol (2.5 g, 9.43 mmol) was dropped into the reaction mixture. Within 5 minutes a solid began to come out of solution. After a minimum of 3 h, the reaction was filtered and washed 3× with cold MeOH, yielding 2.874 g (8.49 mmol, 90%) of pure product after drying. 1H NMR (CDCl3): d 7.23 (d, J=8.8 Hz, 2H, AA′ of AA′ BB′ aromatic system), 6.85 (d, J=8.8 Hz, 2H, BB′ of AA′ BB′ aromatic system), 3.80 (s, 3H, methoxy), 3.66 (s, 2H, benzyl), 3.64 (dt, J1=6.6 Hz, J2=5.5 Hz, 2H, RCH2OH), 2.40 (t, J=7.3 Hz, 2H, RSCH2R), 1.50–1.65 (cm, 4H, CH2 b to heteroatoms), 1.2–1.4 (cm, 16H, bulk methylenes). After a few minutes After a minimum of 3 h, the reaction was filtered washed 3× with cold MeOH
来源 ID: ord-96b3cf9eec9341c2a75d9f25788a4a8a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1-Phenyl-1H-tetrazole-5-thiol, 12-bromododecan-1-ol and anhydrous potassium carbonate were mixed together in acetone for 18 hrs at room temperature to provide 12-(1-phenyl-1H-tetrazol-5-ylsulfanyl)-dodecan-1-ol in 77% yield following work up and recrystallisation. Ammonium molybdate (VI) tetrahydrate in 35% H2O2 were added to a stirred solution of the solid in THF IMS (500 ml) at 10° C. and stirred at room temperature for 20 hrs. Work-up and crystallisation gave a white solid (m.p.: 56-58° C.), 12-(1-phenyl-1H-tetrazol-5-sulfonyl)-dodecan-1-ol in 95% yield. N-Bromosuccinimide was added to a solution of the alcohol and triphenylphosphine in dichloromethane and the reaction stirred at room temperature for 75 min. Work-up and purification by chromatography provided a white solid (m.p.: 63-65° C.), 5-(12-bromo-dodecane-1-sulfonyl)-1-phenyl-1H-tetrazole in 72% yield.
来源 ID: ord-4fde77b1a7f646c4aa2a80d2773f6960反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b5cb7f5567294fc5ad7fb1824458fa7f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b5cb7f5567294fc5ad7fb1824458fa7fPubChem 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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