2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

Base Information

Chemical Name:2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene
CAS No.:884512-28-1
Molecular Formula:C₂₈H₄₉NO₅Si
Molecular Weight:507.786
Hs Code.:

Synonyms:2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

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Chemical Property of 2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

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Technology Process of 2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

There total 6 articles about 2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene 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: 47.0%

: (2-hydroxyphenyI)((R)-N-Boc-piperidin-3-yI)methanone

: (2-tert-butyldimethylsiloxyphenyl)((R)-N-Boc-piperidin-3-yl)methanone

: 634590-61-7
(4-methoxybutyl)magnesium chloride

: 2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)phenol

: 884512-28-1
2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

Guidance literature:: (2-hydroxyphenyI)((R)-N-Boc-piperidin-3-yI)methanone; (2-tert-butyldimethylsiloxyphenyl)((R)-N-Boc-piperidin-3-yl)methanone; (4-methoxybutyl)magnesium chloride; In tetrahydrofuran; at 20 ℃; for 2h;

With ammonium chloride; In tetrahydrofuran; water;

Reference yield:

: 163438-09-3
(R)-1-Boc-nipecotic acid

: 884512-28-1
2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

2.1: tert.-butyl lithium / hexanes; diethyl ether / 0.5 h / -78 °C

2.2: 2 h / -78 - 20 °C

3.1: tetrahydrofuran / 2 h / 20 °C

With tert.-butyl lithium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexanes; diethyl ether; dichloromethane;

Reference yield:

: 884510-86-5
(R)-tert-butyl 3-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate

: 884512-28-1
2-((S)-1-hydroxy-5-methoxy-1-((R)-N-Boc-piperidin-3-yl)pentyl)[tert-butyldimethylsiloxy]benzene

Guidance literature:: Multi-step reaction with 2 steps

1.1: tert.-butyl lithium / hexanes; diethyl ether / 0.5 h / -78 °C

1.2: 2 h / -78 - 20 °C

2.1: tetrahydrofuran / 2 h / 20 °C

With tert.-butyl lithium; In tetrahydrofuran; hexanes; diethyl ether;