(S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester
CAS No.:1229652-77-0
Molecular Formula:C₃₀H₃₅NO₄Si
Molecular Weight:501.698
Hs Code.:

Synonyms:(S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

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Chemical Property of (S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

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Technology Process of (S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

There total 1 articles about (S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester 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: 92.0%

: 1229652-93-0
(S)-[2-(tert-butyldiphenylsilanyloxymethyl)-5-hydroxypentyl]carbamic acid benzyl ester

: 1229652-77-0
(S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; In dichloromethane; water; at 20 ℃; for 2h;
DOI:10.1021/ol100928v

Reference yield:

: 34837-55-3
Phenylselenyl bromide

: 1229652-77-0
(S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester

: 1229652-91-8
C₃₆H₃₉NO₄SeSi

Guidance literature:: (S)-5-(tert-butyldiphenylsilanyloxymethyl)-2-oxopiperidine-1-carboxylic acid benzyl ester; With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

Phenylselenyl bromide; In tetrahydrofuran; hexane; for 1h;
DOI:10.1021/ol100928v