反应 #4027393
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-103524389f6249cebd5203218fe62983暂无可渲染的结构数据
CC(CNC(=O)C1=CC=CC=C1)O产品信息
N-(2-羟基丙基)苯甲酰胺(CAS 23054-66-2)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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合成路线数据
11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-103524389f6249cebd5203218fe62983反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-48cef175d4194e06b8c7970b8395408e反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepare a solution of N-(2-hydroxypropyl)benzamide (8.22 g, 45.9 mmol) in methylene chloride (100 mL). Add N-methylmorpholine N-oxide (7.0 g, 60.0 mmol) followed by powdered 4 Å molecular sieves. Cool the mixture to 0° C. and add tetra-n-propylammonium perruthenate in one portion. Stir the mixture for 30 minutes and then warm to room temperature for 1 hour and filter through Celite®. Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate to afford 6.1 g of N-(2-oxopropyl)benzamide as a white solid. MS: m/e=178 (MH+) warm to room temperature for 1 hour filter through Celite® Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate
来源 ID: ord-9ebfa026cad1413e977caaa07a299728反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepare a solution of N-(2-hydroxypropyl)benzamide (8.22 g, 45.9 mmol) in methylene chloride (100 mL). Add N-methylmorpholine N-oxide (7.0 g, 60.0 mmol) followed by powdered 4 Å molecular sieves. Cool the mixture to 0° C. and add tetra-n-propylammonium perruthenate in one portion. Stir the mixture for 30 minutes and then warm to room temperature for 1 hour and filter through Celite®. Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate to afford 6.1 g of N-(2-oxopropyl)benzamide as a white solid. MS: m/e=178 (MH+) warm to room temperature for 1 hour filter through Celite® Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate
来源 ID: ord-9ebfa026cad1413e977caaa07a299728反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepare a solution of 1-amino-2-propanol (5.0 g, 66.6 mmol) in methylene chloride (250 mL) at 0° C. under nitrogen. Add Hünig's Base (11.6 mL, 66.6 mmol) followed by benzoyl chloride (7.7 mL, 66.6 mmol). Warm the reaction mixture to room temperature and stir overnight. Wash the solution sequentially with brine (100 mL) and 1M HCl (75 mL), dry (Na2SO4), filter, and concentrate to afford 10.0 g of N-(2-hydroxypropyl)benzamide. MS: m/e=180 (MH+) Wash the solution sequentially with brine (100 mL) and 1M HCl (75 mL) dry (Na2SO4) filter concentrate
来源 ID: ord-1720d19d049141adb3d8182c3e3dac2d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-103524389f6249cebd5203218fe62983反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-48cef175d4194e06b8c7970b8395408e反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepare a solution of N-(2-hydroxypropyl)benzamide (8.22 g, 45.9 mmol) in methylene chloride (100 mL). Add N-methylmorpholine N-oxide (7.0 g, 60.0 mmol) followed by powdered 4 Å molecular sieves. Cool the mixture to 0° C. and add tetra-n-propylammonium perruthenate in one portion. Stir the mixture for 30 minutes and then warm to room temperature for 1 hour and filter through Celite®. Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate to afford 6.1 g of N-(2-oxopropyl)benzamide as a white solid. MS: m/e=178 (MH+) warm to room temperature for 1 hour filter through Celite® Concentrate the filtrate and flash-chromatograph on silica gel eluting with 100% ethyl acetate
来源 ID: ord-9ebfa026cad1413e977caaa07a299728反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepare a solution of 1-amino-2-propanol (5.0 g, 66.6 mmol) in methylene chloride (250 mL) at 0° C. under nitrogen. Add Hünig's Base (11.6 mL, 66.6 mmol) followed by benzoyl chloride (7.7 mL, 66.6 mmol). Warm the reaction mixture to room temperature and stir overnight. Wash the solution sequentially with brine (100 mL) and 1M HCl (75 mL), dry (Na2SO4), filter, and concentrate to afford 10.0 g of N-(2-hydroxypropyl)benzamide. MS: m/e=180 (MH+) Wash the solution sequentially with brine (100 mL) and 1M HCl (75 mL) dry (Na2SO4) filter concentrate
来源 ID: ord-1720d19d049141adb3d8182c3e3dac2d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-103524389f6249cebd5203218fe62983反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-48cef175d4194e06b8c7970b8395408ePubChem References
以下资料来自该化合物的公开数据库参考记录。
