反应 #4133318
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-a1ace13d61e043af9ca45b794bcbe08b暂无可渲染的结构数据
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2-(2-氯乙氧基)乙醇(CAS 52137-03-8)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-a1ace13d61e043af9ca45b794bcbe08b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-440f202a51a44a58a546f07ac91ae8a6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d4d3be5f44cc46fab83a05a4cb44513c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-53e3c98e21044b9a8a4343037c7ac5ec反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-631bbb60532448e9a0b9b9d8762247aa反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bd31cf4bda134528830db16e9b7247b9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a4a1e96bc3a046d2b6cc56a5566a3b6d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-849c38469205436b95496e375f8ff2d0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d81b069b0c5d472cae4d9e612d268a90反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f37b97c236e54382bb6f9e2ca2bdeae1反应条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-(2-chloroethoxy)ethanol 14 (5 mL, 47.4 mmol) in N,N-dimethylformamide (35 mL) was added potassium phthalimide 2 (8.8 g, 47.51 mmol), and the reaction mixture was stirred for 20 h at 70° C. The mixture was concentrated and then diluted with dichloromethane (300 mL), and the organic layer was washed with water, dried, and concentrated. The residue was purified by flash column chromatography (3:2 to 2:3 hexane-ethyl acetate) to give compound 15 as a white solid (7.15 g, 64.17%) having an RF of 0.12 (solvent 3:2 hexane-ethyl acetate). See FIG. 9. The mixture was concentrated diluted with dichloromethane (300 mL) the organic layer was washed with water dried concentrated The residue was purified by flash column chromatography (3:2 to 2:3 hexane-ethyl acetate)
来源 ID: ord-cf405ceb7bdf43ffb257a0be49cbc372反应条件: temp:85.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 400 mg (0.746 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamide (Example 53), 0.18 ml (1.7 mmol) 2-(2-chloroethoxy)-ethanol and 0.189 g (1.35 mmol) potassium carbonate in 8 ml acetonitrile was stirred at 85° C. for 48 h. After cooling to room temperature 40 ml 1 N sodium hydroxide solution were added. Extraction with 3 60-ml portions of dichloromethane, drying with sodium sulfate and concentration gave 528 mg of the crude product. Flash column chromatography afforded 300 mg (64.4%) of the title compound as a light-brown solid. were added Extraction with 3 60-ml portions of dichloromethane drying with sodium sulfate and concentration gave 528 mg of the crude product
来源 ID: ord-f700a9ab02e34db28dc82b73bf8a7668PubChem References
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