反应 #4139119
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-acf973a020a04cfeab66432a2440bec1暂无可渲染的结构数据
C1=C(C=C(C=C1Br)Br)CBr产品信息
1,3-二溴-5-(溴甲基)苯(CAS 56908-88-4)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-acf973a020a04cfeab66432a2440bec1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0278821f7180408e8347d9755367a954反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-97af68b6367745e281644bfa00d3db71反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a35e2bb8e81a419882bec1a844dc86de反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d0ccce360c5f4006b5ccd356abe2e846反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07e203fd9f7b4e259ee85f5c2fa2a59c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3,5-dibromobenzylbromide (Lancaster) (20 g, 0.061 mole) in H2O (27 mL) and glacial acetic acid (27 mL) was added hexamethylenetetramine (Aldrich). The reaction mixture was heated at reflux for 2 hours. Concentrated HCl (22 mL) was then added and the refluxing was continued for 30 minutes. After cooling to room temperature, the reaction mixture was poured into H2O (230 mL) and stirred for 10 minutes. The resulting precipitate was filtered, washed with H2O and dried to yield 3,5-dibromobenzaldehyde (11.45 g) as a white solid. MS and NMR were consistent with the desired structure. The reaction mixture was heated at reflux for 2 hours The resulting precipitate was filtered washed with H2O dried
来源 ID: ord-f3c898486bb044c3a3b6b92432ed6315反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-acf973a020a04cfeab66432a2440bec1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-acf973a020a04cfeab66432a2440bec1反应条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 1,3-dibromo-5-(bromomethyl)benzene (1.1 g, ˜3.3 mmol) and potassium phthalimide (0.62 g, 3.3 mmol) in DMF (10 ml) was heated at 120° C. for 2 hours. After cooled down, a white solid precipitated. The solid was filtered and washed with ethanol, then dried in vacuum. 2-(3,5-dibromobenzyl)isoindoline-1,3-dione (1.1 g, 83%) was obtained as white solid. After cooled down a white solid precipitated The solid was filtered washed with ethanol dried in vacuum
来源 ID: ord-6e9cde365f1144f59c5e14c9be0faa94反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Step H1. A mixture of 3,5-dibromo-toluene (4.25 g, 17 mmol), NBS (3 g, 17 mmol), and AIBN (150 mg) in carbon tetrachloride (50 mL) was heated at 80° C. for 3 hours. The resulting mixture was run through a silicon gel column with dichloromethane as the eluant. The fraction was collected and solvent was removed by rotovap, crude 1,3-dibromo-5-(bromomethyl)benzene was obtained as a white residue. The fraction was collected solvent was removed by rotovap
来源 ID: ord-b6e3a773b1124b5f9d14e4b3c6096d1a反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Step H1. A mixture of 3,5-dibromo-toluene (4.25 g, 17 mmol), NBS (3 g, 17 mmol), and AIBN (150 mg) in carbon tetrachloride (50 mL) was heated at 80° C. for 3 hours. The resulting mixture was run through a silicon gel column with dichloromethane as the eluant. The fraction was collected and solvent was removed by rotovap, crude 1,3-dibromo-5-(bromomethyl)benzene was obtained as a white residue. The fraction was collected solvent was removed by rotovap
来源 ID: ord-b6e3a773b1124b5f9d14e4b3c6096d1aPubChem References
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