(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

Base Information

Chemical Name:(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol
CAS No.:1574555-38-6
Molecular Formula:C₂₄H₃₅Cl₂NO₂Si
Molecular Weight:468.539
Hs Code.:

Synonyms:(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

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Chemical Property of (R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

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Technology Process of (R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

There total 6 articles about (R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 1429387-88-1
(1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethanamine

: 106-88-7,3760-95-0,30608-62-9,55555-96-9
(R)-(+)-1,2-epoxybutane

: 1574555-38-6
(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

Guidance literature:: With ytterbium(III) triflate; In acetonitrile; at 130 ℃; for 3h; Microwave irradiation; Inert atmosphere;
DOI:10.1021/jm401767k

Reference yield:

: rac-(1R,2R)-2-amino-1-(3-chlorophenyl)-2-(4-chlorophenyl)ethanol hydrochloride

: 1574555-38-6
(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / Inert atmosphere

1.2: Inert atmosphere; Reflux

2.1: 1H-imidazole / dichloromethane / 25 °C / Inert atmosphere

3.1: ytterbium(III) triflate / acetonitrile / 3 h / 130 °C / Microwave irradiation; Inert atmosphere

With 1H-imidazole; sodium hydroxide; ytterbium(III) triflate; In dichloromethane; acetonitrile;
DOI:10.1021/jm401767k

Reference yield:

: C₂₀H₂₅Cl₂NO₃Si

: 1574555-38-6
(R)-1-(((1R,2R)-2-((tert-butyldimethylsilyl)oxy)-2-(3-chlorophenyl)-1-(4-chlorophenyl)ethyl)amino)butan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride; zinc / water / Inert atmosphere

2.1: sodium hydroxide / Inert atmosphere

2.2: Inert atmosphere; Reflux

3.1: 1H-imidazole / dichloromethane / 25 °C / Inert atmosphere

4.1: ytterbium(III) triflate / acetonitrile / 3 h / 130 °C / Microwave irradiation; Inert atmosphere

With 1H-imidazole; hydrogenchloride; sodium hydroxide; ytterbium(III) triflate; zinc; In dichloromethane; water; acetonitrile;
DOI:10.1021/jm401767k