反応 #4173106
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2ed69aefdbfe4c1a9b19199a890be899表示可能な構造データがありません
C1=CC=C(C(=C1)C=O)C#N製品情報
2-formylbenzonitrile (CAS 7468-67-9) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 101209
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2ed69aefdbfe4c1a9b19199a890be899反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-04deb8387c564308afdc670f8ecb0405反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cd755c065d534477bdffca3cf5cfe238反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6fc0e4bcaed54909b9c79611c1356725反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-93a1290f20224790a9dbf700f76c7adc反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-59101ab56cd448bda527fb1f2ca3d2de反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-7411f13c30544adf82f7ba101a5a5f7b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2ed69aefdbfe4c1a9b19199a890be899反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-fedf5bc000f243f1b3435852131f5c5c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-fedf5bc000f243f1b3435852131f5c5c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-2185f00a59a84529b296bfcd938657d4反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-2185f00a59a84529b296bfcd938657d4PubChem References
化合物の公開データベース記録に掲載された情報源です。
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