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HRID 1682726생성일: 2026년 10월 25일

Benzene → 2-[2-(4-Methoxycarbonylmethylphenoxy)-1-methylethyl]amino-1-(3-bromophenyl)ethanol

https://huagongshe.com/reaction/1682726

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Methyl 4-(2-oxopropoxy)phenylacetateHCID 21832178—
반응물2-Amino-1-(3-bromophenyl)ethan-1-olHCID 22021067—
용매MethanolHCID 887—
생성물2-[2-(4-Methoxycarbonylmethylphenoxy)-1-methylethyl]amino-1-(3-bromophenyl)ethanolHCID 5384648656.8%

반응 단계

Following a procedure similar to that described in Example 3, but using 3.0 g of 2-amino-1-(3-bromophenyl)ethanol (prepared as described in Preparation 41), 3.67 g of methyl 4-(2-oxopropoxy)phenylacetate (prepared as described in Preparation 3), 80 ml of benzene, 60 ml of absolute methanol and 3.1 g of sodium cyanoborohydride, and then purifying the reaction product by column chromatography through silica gel, using ethyl acetate as the eluent, 3.33 g of the title compound were obtained having an Rf=0.25 (thin layer chromatography over silica gel, using ethyl acetate as the developing solvent).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05635534
출처 데이터셋uspto-grants-1997_06
ORD IDord-588ff5745cbb46829d703ae630ec95f2
출처 메모uspto-grants-1997_06