反应 #4157449
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-224ce505fceb4bad9f63d210136d017c暂无可渲染的结构数据
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2-(N-Boc-N-甲基氨基)乙醇(CAS 57561-39-4)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-224ce505fceb4bad9f63d210136d017c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-26975ced435847b89b949795568739d6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b6c11597629a4bf6ba5d5908404022c8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f2e2f25c1838499b9315ae634e1033ad反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d59be45ed31428eadbd9d1e253935e8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-502463c62ff1444d821762caeb0a2193反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f48328c4b9374993a31bf7bf298533b2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ff85f4cba9f7492d9a1aa3834a96a483反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: [2-(2-Dibenzylamino-ethoxy)-ethyl]-methyl-carbamic acid tert-butyl ester (200 mg) was prepared by following General Procedure S starting from dibenzyl-(2-chloro-ethyl)-amine (400 mg), (2-hydroxy-ethyl)-methyl-carbamic acid tert-butyl ester (525 mg), 50% (w/w) KOH solution (1.8 mL) and tetrabutylammonium bromide (57.7 mg) in dioxane (1.8 mL).
来源 ID: ord-843280e7221d4553b5e61ad4043f6770反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Methanesulphonyl chloride (2.98 ml, 38.6 mmol) was added to an ice-cold solution of tert-butyl 2-hydroxyethyl(methyl)carbamate (Synth. Commun. 1993; 23(17); 2443) (4.5 g, 25.7 mmol) in pyridine (40 ml), and the reaction stirred for 2 hours. The solution was poured into water (150 ml), and extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with 10% aqueous citric acid solution, dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (34:66 to 40:60) to give the title compound, 1.0 g. extracted with ethyl acetate (2×50 ml) The combined organic extracts were washed with 10% aqueous citric acid solution dried (MgSO4) evaporated under reduced pressure The crude product was purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (34:66 to 40:60)
来源 ID: ord-779c975a8a6e45a798e7b1f314274824反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-224ce505fceb4bad9f63d210136d017c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-26975ced435847b89b949795568739d6PubChem References
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