反应 #4142478
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-a0424baac2414bb484f1d4970564fcb7暂无可渲染的结构数据
CC(C)(C)OC(=O)NNCC1=CC=CC=C1产品信息
2-N-BOC-1-苄基肼(CAS 53370-84-6)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-a0424baac2414bb484f1d4970564fcb7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9ecc0ee730264ab0a88dd431aee33929反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N'-benzylhydrazinecarboxylic acid tert-butyl ester (2.5 g, 11.8 mmol) in 99% ethanol (40 ml) was added ethyl isocyanate (1.1 g, 15.2 mmol) and the mixture was stirred for 2 h. Then the mixture was concentrated in vacuo and chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2 to give 3.0 g of 2-benzyl-1-tert-butoxycarbonyl-4-ethylsemicarbazide. Then the mixture was concentrated in vacuo chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2
来源 ID: ord-85acc104d7f642ba91e1696dbe5b675b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N'-benzylidenehydrazinecarboxylic acid tert-butyl ester (2.7 g, 12.3 mmol) in tetrahydrofuran (100 ml) was added 10% palladium on carbon (0.3 g) and the mixture was hydrogenated with 280 ml of hydrogen for 40 min at atmospheric pressure. The mixture was filtered through a plug of celite and the filtrate was concentrated in vacuo to give 2.63 g of N'-benzylhydrazinecarboxylic acid tert-butyl ester. The mixture was filtered through a plug of celite the filtrate was concentrated in vacuo
来源 ID: ord-64abae71a23f43dcb6291a69c175bcf9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a0424baac2414bb484f1d4970564fcb7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a0424baac2414bb484f1d4970564fcb7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N′-benzylhydrazinecarboxylic acid tert-butyl ester (2.5 g, 11.8 mmol) in 99% ethanol (40 ml) was added ethyl isocyanate (1.1 g, 15.2 mmol) and the mixture was stirred for 2 h. Then the mixture was concentrated in vacuo and chromatographed on silica (20 g) with petrol etherlethyl acetate 3:2 to give 3.0 g of 2-benzyl-1-tert-butoxycarbonyl-4-ethylsemicarbazide. Then the mixture was concentrated in vacuo chromatographed on silica (20 g) with petrol etherlethyl acetate 3:2
来源 ID: ord-efde3771051546d5a2d33dba430f60d2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N′-benzylidenehydrazinecarboxylic acid tert-butyl ester (2.7 g, 12.3 mmol) in tetrahydrofuran (100 ml) was added 10% palladium on carbon (0.3 g) and the mixture was hydrogenated with 280 ml of hydrogen for 40 min at atmospheric pressure. The mixture was filtered through a plug of celite and the filtrate was concentrated in vacuo to give 2.63 9 of N′-benzylhydrazinecarboxylic acid tert-butyl ester. The mixture was filtered through a plug of celite the filtrate was concentrated in vacuo
来源 ID: ord-033cf671250c4eaabbf678e836e3365e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N′-benzylidenehydrazinecarboxylic acid tert-butyl ester (2.7 g, 12.3 mmol) in tetrahydrofuran (100 ml) was added 10% palladium on carbon (0.3 g) and the mixture was hydrogenated with 280 ml of hydrogen for 40 min at atmospheric pressure. The mixture was filtered through a plug of celite and the filtrate was concentrated in vacuo to give 2.63 9 of N′-benzylhydrazinecarboxylic acid tert-butyl ester. The mixture was filtered through a plug of celite the filtrate was concentrated in vacuo
来源 ID: ord-033cf671250c4eaabbf678e836e3365e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: ##STR186## To a solution of N'-benzylhydrazinecarboxylic acid tert-butyl ester (2.5 g, 11.8 mmol) in 99% ethanol (40 ml) was added ethyl isocyanate (1.1 g, 15.2 mmol) and the mixture was stirred for 2 h. Then the mixture was concentrated in vacuo and chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2 to give 3.0 g of 2-benzyl-1-tert-butoxycarbonyl-4-ethylsemicarbazide. Then the mixture was concentrated in vacuo chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2
来源 ID: ord-323f6c6f1e4148eb8b1e3d667a8862be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: ##STR186## To a solution of N'-benzylhydrazinecarboxylic acid tert-butyl ester (2.5 g, 11.8 mmol) in 99% ethanol (40 ml) was added ethyl isocyanate (1.1 g, 15.2 mmol) and the mixture was stirred for 2 h. Then the mixture was concentrated in vacuo and chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2 to give 3.0 g of 2-benzyl-1-tert-butoxycarbonyl-4-ethylsemicarbazide. Then the mixture was concentrated in vacuo chromatographed on silica (20 g) with petrol ether/ethyl acetate 3:2
来源 ID: ord-323f6c6f1e4148eb8b1e3d667a8862be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: ##STR185## To a solution of N'-benzylidenehydrazinecarboxylic acid tert-butyl ester (2.7 g, 12.3 mmol) in tetrahydrofuran (100 ml) was added 10% palladium on carbon (0.3 g) and the mixture was hydrogenated with 280 ml of hydrogen for 40 min at atmospheric pressure. The mixture was filtered through a plug of celite and the filtrate was concentrated in vacuo to give 2.63 g of N'-benzylhydrazinecarboxylic acid tert-butyl ester. The mixture was filtered through a plug of celite the filtrate was concentrated in vacuo
来源 ID: ord-7885615e5266416ba13cfce617241f7ePubChem References
以下资料来自该化合物的公开数据库参考记录。
