反应 #3873395
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-9661f42ae72a4de784496fd876c66c02暂无可渲染的结构数据
C1=CC=C2C(=C1)C(=CO2)CCNC=O产品信息
N-[2-(1-苯并呋喃-3-基)乙基]甲酰胺(CAS 100480-86-2)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9661f42ae72a4de784496fd876c66c02反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2 N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-a25e39a8707c4822b86cd8e84a9fce96反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2 N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-a25e39a8707c4822b86cd8e84a9fce96反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-e3353796cc544f0db271fd22430ad475反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-e3353796cc544f0db271fd22430ad475反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-539c1345ae2040afb4f9022e288362d6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-539c1345ae2040afb4f9022e288362d6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4) , filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-ef7cbc829ce44fc89771a48e1bca533d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 grams (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 milliliters of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl extracted with methylene chloride, the latter washed with 5% sodium hydroxide, dried, filtered and concentrated to obtain the product. extracted with methylene chloride the latter washed with 5% sodium hydroxide dried filtered concentrated to obtain the product
来源 ID: ord-4ac262eabca34b2da9776e6118807875反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 g (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (MgSO4), filtered and concentrated to give 2.70 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (MgSO4) filtered concentrated
来源 ID: ord-9b18f248c70e4a0392e77af9b435df2f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 121 g of 2-(3-benzo[b]furanyl)-ethylamine and 300 mL of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl and washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v), dried (Na2SO4), charcoaled and concentrated to give 118 g of product. washed with methylene chloride which in turn was washed with 5% sodium hydroxide (w/v) dried (Na2SO4) concentrated
来源 ID: ord-9f4fdd9381e043b59fde473ab24256e6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2.35 grams (0.015 mole) of 2-(3-benzo[b]furanyl)ethylamine and 5 milliliters of ethyl formate was heated at 60° C. for 3 hours, poured into 2N HCl extracted with methylene chloride, the latter washed with 5% sodium hydroxide, dried, filtered and concentrated to obtain the product. extracted with methylene chloride the latter washed with 5% sodium hydroxide dried filtered concentrated to obtain the product
来源 ID: ord-46f07745db6c4d65a5d0c9b390d38e79PubChem References
以下资料来自该化合物的公开数据库参考记录。
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