反応 #4169617
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-cc4994ec6f7b482b842656cce2327376表示可能な構造データがありません
CC(CCC1=CC=C(C=C1)OC)N製品情報
4-(4-methoxyphenyl)butan-2-amine (CAS 51062-15-8) 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 410202
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
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cc4994ec6f7b482b842656cce2327376反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cc4994ec6f7b482b842656cce2327376反応条件: temp:115.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol. after washing twice each time with 200 ml of water the benzene layer was purified by a silica gel column chromatography (eluate a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)
ソース ID: ord-4d1c2a077466449880af350d04427420反応条件: temp:115.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol. after washing twice each time with 200 ml of water the benzene layer was purified by a silica gel column chromatography (eluate a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)
ソース ID: ord-4d1c2a077466449880af350d04427420反応条件: temp:115.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol. after washing twice each time with 200 ml of water the benzene layer was purified by a silica gel column chromatography (eluate a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)
ソース ID: ord-ad4099130e324647abf22ee93531e7ca反応条件: temp:115.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol. after washing twice each time with 200 ml of water the benzene layer was purified by a silica gel column chromatography (eluate a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)
ソース ID: ord-eebc6ba1663b45e2aa58c09b544997f8反応条件: temp:115.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol. after washing twice each time with 200 ml of water the benzene layer was purified by a silica gel column chromatography (eluate a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)
ソース ID: ord-4d1c2a077466449880af350d04427420PubChem References
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