反应 #4173106
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-2ed69aefdbfe4c1a9b19199a890be899暂无可渲染的结构数据
C1=CC=C(C(=C1)C=O)C#N产品信息
2-甲酰基苄腈(CAS 7468-67-9)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-2ed69aefdbfe4c1a9b19199a890be899反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-04deb8387c564308afdc670f8ecb0405反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cd755c065d534477bdffca3cf5cfe238反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6fc0e4bcaed54909b9c79611c1356725反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-93a1290f20224790a9dbf700f76c7adc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-59101ab56cd448bda527fb1f2ca3d2de反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7411f13c30544adf82f7ba101a5a5f7b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ed69aefdbfe4c1a9b19199a890be899反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-amino-p-cresol (9.8 g) and 2-formylbenzonitrile (10.5 g) in ethanol (160 ml) was allowed to stand for 20 hours. The precipitated solid was filtered off and washed with ethanol (30 ml) to give 2-hydroxy-5-methyl-N-(2-cyanobenzylidene)aniline (C) (3.1 g), m.p. 135°-138° C.; NMR: 2.35(s, 3H), 6.95(d, 1H), 7.1(dd, 1H), 7.2(s & br s, 2H), 7.55(dt, 1H), 7.7(dt, 1H), 7.8(dd, 1H) 8.1(dd, 1H), 8.9(s, 1H). The precipitated solid was filtered off washed with ethanol (30 ml)
来源 ID: ord-fedf5bc000f243f1b3435852131f5c5c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2-amino-p-cresol (9.8 g) and 2-formylbenzonitrile (10.5 g) in ethanol (160 ml) was allowed to stand for 20 hours. The precipitated solid was filtered off and washed with ethanol (30 ml) to give 2-hydroxy-5-methyl-N-(2-cyanobenzylidene)aniline (C) (3.1 g), m.p. 135°-138° C.; NMR: 2.35(s, 3H), 6.95(d, 1H), 7.1(dd, 1H), 7.2(s & br s, 2H), 7.55(dt, 1H), 7.7(dt, 1H), 7.8(dd, 1H) 8.1(dd, 1H), 8.9(s, 1H). The precipitated solid was filtered off washed with ethanol (30 ml)
来源 ID: ord-fedf5bc000f243f1b3435852131f5c5c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Upon heating a solution of 6.5 g of 2-cyanobenzaldehyde, 5.6 g of cyclohexane-1,3-dione and 6.5 g of amidinoacetic acid ethyl ester in 100 ml of ethanol for 5 hours, 2-amino-4-(2-cyanophenyl)-1,4,5,6,7,8-hexahydro-5-oxoquinoline-3-carboxylic acid ethyl ester of melting point 165°C (ethanol) is obtained.
来源 ID: ord-2185f00a59a84529b296bfcd938657d4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Upon heating a solution of 6.5 g of 2-cyanobenzaldehyde, 5.6 g of cyclohexane-1,3-dione and 6.5 g of amidinoacetic acid ethyl ester in 100 ml of ethanol for 5 hours, 2-amino-4-(2-cyanophenyl)-1,4,5,6,7,8-hexahydro-5-oxoquinoline-3-carboxylic acid ethyl ester of melting point 165°C (ethanol) is obtained.
来源 ID: ord-2185f00a59a84529b296bfcd938657d4PubChem 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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