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HRID 1901183作成日:2026年10月25日

Benzene → 2-[2-(4-Methoxycarbonylmethylphenoxy)-1-methylethyl]amino-1-(3,5-dichlorophenyl)ethanol

https://huagongshe.com/reaction/1901183

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物2-Amino-1-(3,5-dichlorophenyl)ethan-1-olHCID 3782382—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Methyl 4-(2-oxopropoxy)phenylacetateHCID 21832178—
溶媒MethanolHCID 887—
生成物2-[2-(4-Methoxycarbonylmethylphenoxy)-1-methylethyl]amino-1-(3,5-dichlorophenyl)ethanolHCID 1904483760%

反応手順

Following a procedure similar to that described in Example 3, but using 3.0 g of 2-amino-1-(3,5-dichlorophenyl)ethanol (prepared as described in Preparation 39), 3.87 g of methyl 4-(2-oxopropoxy)phenylacetate (prepared as described in Preparation 3), 80 ml of benzene, 60 ml of absolute methanol and 2.9 g of sodium cyanoborohydride, and then purifying the reaction product by column chromatography through silica gel, using ethyl acetate as the eluent, 3.6 g of the title compound were obtained, having an Rf=0.51 (thin layer chromatography over silica gel, using ethyl acetate as the developing solvent).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05576340
出典データセットuspto-grants-1996_11
ORD IDord-82cb103cf8714c66aa61f03f4d3513e6
出典メモuspto-grants-1996_11