toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

Base Information

Chemical Name:toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester
CAS No.:906079-26-3
Molecular Formula:C₃₃H₅₄O₆SSi₂
Molecular Weight:635.025
Hs Code.:

toluene-4-sulfonic acid 6-(<i>tert</i>-butyl-dimethyl-silanyloxy)-2-(<i>tert</i>-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

Synonyms:toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

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Chemical Property of toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

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Technology Process of toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

There total 3 articles about toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl 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:

: 906079-24-1
acetic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

: 906079-26-3
toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / ethylmagnesium bromide / tetrahydrofuran / 1.5 h / 20 °C

2: 86 percent / triethylamine; 4-dimethyaminopyridine / CH₂Cl₂ / 288 h / 20 °C

With dmap; ethylmagnesium bromide; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2006.03.035

Reference yield:

: 105857-77-0
2,2-Bis-hydroxymethyl-5,7,8-trimethyl-chroman-6-ol

: 906079-26-3
toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 60 percent / Candida antarctica lipase B; molecular sieves 3 Angstroem / diethyl ether / 2 h / 20 °C

2: 95 percent / imidazole / dimethylformamide / 24 h / 20 °C

3: 97 percent / ethylmagnesium bromide / tetrahydrofuran / 1.5 h / 20 °C

4: 86 percent / triethylamine; 4-dimethyaminopyridine / CH₂Cl₂ / 288 h / 20 °C

With 1H-imidazole; dmap; Candida antarctica lipase B; 3 A molecular sieve; ethylmagnesium bromide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2006.03.035

Reference yield:

: 479353-37-2
Acetic acid (S)-6-hydroxy-2-hydroxymethyl-5,7,8-trimethyl-chroman-2-ylmethyl ester

: 906079-26-3
toluene-4-sulfonic acid 6-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-5,7,8-trimethyl-chroman-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / imidazole / dimethylformamide / 24 h / 20 °C

2: 97 percent / ethylmagnesium bromide / tetrahydrofuran / 1.5 h / 20 °C

3: 86 percent / triethylamine; 4-dimethyaminopyridine / CH₂Cl₂ / 288 h / 20 °C

With 1H-imidazole; dmap; ethylmagnesium bromide; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2006.03.035