(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

Base Information

Chemical Name:(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one
CAS No.:1352743-17-9
Molecular Formula:C₂₁H₃₁NO₂Si
Molecular Weight:357.568
Hs Code.:

Synonyms:(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

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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 (S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

Chemical Property:

Purity/Quality:

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Technology Process of (S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

There total 4 articles about (S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one 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:

: 1352743-08-8
(S,Z)-2-(tert-butyldimethylsiloxy)-N-(5-oxohept-3-en-3-yl)-2-phenylacetamide

: 1352743-17-9
(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; triethylamine; In dichloromethane; for 48h; Reflux;
DOI:10.1002/ejoc.201100681

Reference yield:

: 17199-29-0
(S)-Mandelic acid

: 1352743-17-9
(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: 1H-imidazole / tetrahydrofuran / 16 h / 20 °C

2: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 4 h / 20 °C

3: triethylamine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

4: trimethylsilyl trifluoromethanesulfonate; triethylamine / dichloromethane / 48 h / Reflux

With 1H-imidazole; oxalyl dichloride; trimethylsilyl trifluoromethanesulfonate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;
DOI:10.1002/ejoc.201100681

Reference yield:

: 168134-61-0
(2S)-O-(tert-butyldimethylsilyl)mandelolyl chloride

: 1352743-17-9
(S)-2-[(tert-butyldimethylsiloxy)(phenyl)methyl]-6-ethyl-3-methylpyridin-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere

2: trimethylsilyl trifluoromethanesulfonate; triethylamine / dichloromethane / 48 h / Reflux

With trimethylsilyl trifluoromethanesulfonate; triethylamine; In dichloromethane;
DOI:10.1002/ejoc.201100681