反应 #4120393
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a727c406426b49759f885275598e7024暂无可渲染的结构数据
CCCCN(CCCC)CCN产品信息
N,N-二正丁基乙二胺(CAS 3529-09-7)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
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来源 ID: ord-bb5dea5ec1f64f18a3aa913a10d5403d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-nonyl maleimide (0.02 mM) prepared as described in Example 12 above in 2 ml of acetonitrile was treated with one equivalent of triethylamine and one equivalent of N,N-dibutylethylenediamine. The reaction mixture was stirred for six hours and then the acetonitrile was evaporated. The residue obtained was treated with cold aqueous dilute hydrochloric acid solution and ethyl acetate, with stirring for one hour. The ethyl acetate layer was then separated and concentrated to give the desired product. the acetonitrile was evaporated The residue obtained with stirring for one hour The ethyl acetate layer was then separated concentrated
来源 ID: ord-d2a58ec7360943a4acba299008de7e77反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-nonyl maleimide (0.02 mM) prepared as described in Example 12 above in 2 ml of acetonitrile was treated with one equivalent of triethylamine and one equivalent of N,N-dibutylethylenediamine. The reaction mixture was stirred for six hours and then the acetonitrile was evaporated. The residue obtained was treated with cold aqueous dilute hydrochloric acid solution and ethyl acetate, with stirring for one hour. The ethyl acetate layer was then separated and concentrated to give the desired product. the acetonitrile was evaporated The residue obtained with stirring for one hour The ethyl acetate layer was then separated concentrated
来源 ID: ord-d2a58ec7360943a4acba299008de7e77反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Chloro-2-(7-chloro-4-quinolylamino)benzoic acid is converted to the acid chloride which is reacted with 2-(di-n-butylamino)ethylamine as in Example 1 to give the title compound.
来源 ID: ord-861caeb6def9434a8593b2c897e23969PubChem References
以下资料来自该化合物的公开数据库参考记录。
