N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

Base Information

Chemical Name:N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine
CAS No.:1356243-04-3
Molecular Formula:C₂₀H₃₇NOSi
Molecular Weight:335.605
Hs Code.:

Synonyms:N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

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Technology Process of N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

There total 4 articles about N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine 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: 48.0%

: 109-72-8,29786-93-4
n-butyllithium

: 1356243-00-9
N-[(1R)-2-tert-butyldimethylsilyloxy-1-phenylethyl]-N-[(1S)-1-(tributylstannyl)ethyl]benzenesulfonamide

: 1356243-04-3
N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

Guidance literature:: In tetrahydrofuran; at -78 ℃; for 1h;
DOI:10.1021/ol300003f

Reference yield:

: 1015843-40-9
N-[(1R)-2-hydroxy-1-phenylethyl]benzenesulfonamide

: 1356243-04-3
N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: camphor-10-sulfonic acid; toluene-4-sulfonic acid / toluene / Reflux

2.1: copper(l) iodide / diethyl ether / 0.5 h / -78 - -50 °C

2.2: 2 h / -78 °C

3.1: 1H-imidazole / dichloromethane

4.1: tetrahydrofuran / 1 h / -78 °C

With 1H-imidazole; copper(l) iodide; camphor-10-sulfonic acid; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; toluene;
DOI:10.1021/ol300003f

Reference yield:

: 1175711-95-1,1175711-99-5
(2S,4R)-4-phenyl-3-(benzenesulfonyl)-2-(tributylstannyl)-1,3-oxazolidine

: 1356243-04-3
N-[(1R)-2-t-butyldimethylsilyloxy-1-phenylethyl]-N-[1-methylpentyl]amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: copper(l) iodide / diethyl ether / 0.5 h / -78 - -50 °C

1.2: 2 h / -78 °C

2.1: 1H-imidazole / dichloromethane

3.1: tetrahydrofuran / 1 h / -78 °C

With 1H-imidazole; copper(l) iodide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ol300003f