反应 #3871225
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-05693d54397d465bbbb7313ca14536b6暂无可渲染的结构数据
C1=CC=C(C=C1)CCCCCCCl产品信息
1-氯-6-苯基己烷(CAS 71434-68-9)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 522411
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-05693d54397d465bbbb7313ca14536b6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(6-phenylhexyloxy)-1,3-benzenedicarboxaldehyde was prepared from 4-hydroxy-1,3-benzenedicarboxaldehyde and 6-phenylhexyl chloride using the method in Example 1 at a higher reaction temperature of 140° C. at a higher reaction temperature of 140° C.
来源 ID: ord-4fad1b86f9eb46cc876c3d88934cb80b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(6-phenylhexyloxy)-1,3-benzenedicarboxaldehyde was prepared from 4-hydroxy-1,3-benzenedicarboxaldehyde and 6-phenylhexyl chloride using the method in Example 1 at a higher reaction temperature of 140° C. at a higher reaction temperature of 140° C.
来源 ID: ord-4fad1b86f9eb46cc876c3d88934cb80b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To dimethylformamide was added 99 mg of 1-chloro-6-phenylhexane and 152 mg of potassium iodide under ice-cooling, the mixture was allowed to warm up to room temperature and stirred for 20 minutes. Then, 200 mg of 5-(3,5-dichlorophenylthio)-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole (101b)was added, followed by addition of 126 mg of potassium carbonate. Then, the mixture was warmed up to 50° C. and allowed to react for 6 hours. After completion of the reaction, the mixture was diluted with water, extracted with diethyl ether, the extract was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. To thus-obtained oil were added 10 ml of ethanol and 20 ml of 36% hydrochloric acid, and the mixture was stirred at 90° C. for 2 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, an aqueous sodium hydrogen carbonate solution was added, and extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1)to give 81 mg of Compound I-125 (yield 37%). cooling Then, the mixture was warmed up to 50° C. to react for 6 hours After completion of the reaction extracted with diethyl ether the extract was dried over sodium sulfate the solvent was distilled off under reduced pressure To thus-obtained oil the mixture was stirred at 90° C. for 2 hours After completion of the reaction the solvent was distilled off under reduced pressure an aqueous sodium hydrogen carbonate solution was added extracted with ethyl acetate The extract was dried over sodium sulfate the solvent was distilled off under reduced pressure The residue was purified by silica gel chromatography (hexane
来源 ID: ord-c8398caab0fe40efb2520d55dee25cb2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(6-phenylhexyloxy)-1,3-benzenedicarboxaldehyde was prepared from 4-hydroxy-1,3-benzenedicarboxaldehyde and 6-phenylhexyl chloride using the method in Example 1 at a higher reaction temperature of 140° C. at a higher reaction temperature of 140° C.
来源 ID: ord-4fad1b86f9eb46cc876c3d88934cb80bPubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 15733-63-8
CAS 66229-91-2
CAS 223684-81-9
CAS 61221-46-3
CAS 71434-47-4
CAS 306308-12-3
CAS 10304-81-1
CAS 97344-49-5
CAS 69156-39-4
CAS 73756-58-8
CAS 40016-26-0
CAS 104-37-0
