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3-(1,3-二氧戊环-2-基)丙-1-胺（CAS 4388-60-7）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-41f1bfea61284e129ee3a5c257738446反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0d835634626248e8b7804a347563f526反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-41f1bfea61284e129ee3a5c257738446反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 49.85 g (0.38 mol) of 3-[1,3]-dioxolan-2-yl-propylamine and 43.34 g (0.646 mol) of crotono-nitrile are combined in a 200 ml round-bottomed flask and heated at 100° C. for 72 hours. After cooling, the brown mass is diluted with ethyl acetate and washed with water. The organic phase is dried over calcium carbonate and purified by filtration on silica gel (eluent: ethyl acetate). Evaporation of the solvent gives 69.8 g of 3-(3-[1,3]-dioxolan-2-yl-propylamino)butyronitrile as a reddish liquid which is used without further purification in the next stage. After cooling washed with water The organic phase is dried over calcium carbonate purified by filtration on silica gel (eluent: ethyl acetate) Evaporation of the solvent
来源 ID: ord-b17d6a09186343188dcfe257dc075376反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50.1 g (1.32 mol) of lithium aluminium hydride are suspended in 500 ml of ether. Added dropwise to this suspension is a solution of 111.9 g (0.88 mol) of 3-[1,3]-dioxolan-2-yl-propionitrile. The mixture is subsequently heated at reflux for 2.5 hours. After cooling, 50 g of water, 50 g of 10% strength sodium hydroxide solution and a further 150 g of water are added. The mixture is then filtered and the filtrate is dried over calcium chloride and concentrated. The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar). This gives 68.4 g of 3-[1,3]-dioxolan-2-yl-propylamine. Added dropwise to this suspension The mixture is subsequently heated at reflux for 2.5 hours After cooling The mixture is then filtered the filtrate is dried over calcium chloride concentrated The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar)
来源 ID: ord-4e06467f95b147448eeea66ea72a1316反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50.1 g (1.32 mol) of lithium aluminium hydride are suspended in 500 ml of ether. Added dropwise to this suspension is a solution of 111.9 g (0.88 mol) of 3-[1,3]-dioxolan-2-yl-propionitrile. The mixture is subsequently heated at reflux for 2.5 hours. After cooling, 50 g of water, 50 g of 10% strength sodium hydroxide solution and a further 150 g of water are added. The mixture is then filtered and the filtrate is dried over calcium chloride and concentrated. The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar). This gives 68.4 g of 3-[1,3]-dioxolan-2-yl-propylamine. Added dropwise to this suspension The mixture is subsequently heated at reflux for 2.5 hours After cooling The mixture is then filtered the filtrate is dried over calcium chloride concentrated The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar)
来源 ID: ord-4e06467f95b147448eeea66ea72a1316反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 49.85 g (0.38 mol) of 3-[1,3]-dioxolan-2-yl-propylamine and 43.34 g (0.646 mol) of crotononitrile are combined in a 200 ml round-bottomed flask and heated at 100° C. for 72 hours. After cooling, the brown mass is diluted with ethyl acetate and washed with water. The organic phase is dried over calcium carbonate and purified by filtration on silica gel (eluent: ethyl acetate). Evaporation of the solvent gives 69.8 g of 3-(3-[1,3]-dioxolan-2-ylpropylamino)butyronitrile as a reddish liquid which is used without further purification in the next stage. After cooling washed with water The organic phase is dried over calcium carbonate purified by filtration on silica gel (eluent: ethyl acetate) Evaporation of the solvent
来源 ID: ord-260fc75e9e3940c4bf0fe6592cab4abd反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 49.85 g (0.38 mol) of 3-[1,3]-dioxolan-2-yl-propylamine and 43.34 g (0.646 mol) of crotononitrile are combined in a 200 ml round-bottomed flask and heated at 100° C. for 72 hours. After cooling, the brown mass is diluted with ethyl acetate and washed with water. The organic phase is dried over calcium carbonate and purified by filtration on silica gel (eluent: ethyl acetate). Evaporation of the solvent gives 69.8 g of 3-(3-[1,3]-dioxolan-2-ylpropylamino)butyronitrile as a reddish liquid which is used without further purification in the next stage. After cooling washed with water The organic phase is dried over calcium carbonate purified by filtration on silica gel (eluent: ethyl acetate) Evaporation of the solvent
来源 ID: ord-260fc75e9e3940c4bf0fe6592cab4abd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0d835634626248e8b7804a347563f526反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 49.85 g (0.38 mol) of 3-[1,3]-dioxolan-2-yl-propylamine and 43.34 g (0.646 mol) of crotono-nitrile are combined in a 200 ml round-bottomed flask and heated at 100° C. for 72 hours. After cooling, the brown mass is diluted with ethyl acetate and washed with water. The organic phase is dried over calcium carbonate and purified by filtration on silica gel (eluent: ethyl acetate). Evaporation of the solvent gives 69.8 g of 3-(3-[1,3]-dioxolan-2-yl-propylamino)butyronitrile as a reddish liquid which is used without further purification in the next stage. After cooling washed with water The organic phase is dried over calcium carbonate purified by filtration on silica gel (eluent: ethyl acetate) Evaporation of the solvent
来源 ID: ord-b17d6a09186343188dcfe257dc075376反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 50.1 g (1.32 mol) of lithium aluminium hydride are suspended in 500 ml of ether. Added dropwise to this suspension is a solution of 111.9 g (0.88 mol) of 3-[1,3]-dioxolan-2-yl-propionitrile. The mixture is subsequently heated at reflux for 2.5 hours. After cooling, 50 g of water, 50 g of 10% strength sodium hydroxide solution and a further 150 g of water are added. The mixture is then filtered and the filtrate is dried over calcium chloride and concentrated. The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar). This gives 68.4 g of 3-[1,3]-dioxolan-2-yl-propylamine. Added dropwise to this suspension The mixture is subsequently heated at reflux for 2.5 hours After cooling The mixture is then filtered the filtrate is dried over calcium chloride concentrated The orange oil obtained is subsequently distilled under reduced pressure (overhead temperature=46° C., p=0.016 mbar)
来源 ID: ord-4e06467f95b147448eeea66ea72a1316反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 49.85 g (0.38 mol) of 3-[1,3]-dioxolan-2-yl-propylamine and 43.34 g (0.646 mol) of crotononitrile are combined in a 200 ml round-bottomed flask and heated at 100° C. for 72 hours. After cooling, the brown mass is diluted with ethyl acetate and washed with water. The organic phase is dried over calcium carbonate and purified by filtration on silica gel (eluent: ethyl acetate). Evaporation of the solvent gives 69.8 g of 3-(3-[1,3]-dioxolan-2-ylpropylamino)butyronitrile as a reddish liquid which is used without further purification in the next stage. After cooling washed with water The organic phase is dried over calcium carbonate purified by filtration on silica gel (eluent: ethyl acetate) Evaporation of the solvent
来源 ID: ord-260fc75e9e3940c4bf0fe6592cab4abdPubChem References
以下资料来自该化合物的公开数据库参考记录。