formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

Base Information

Chemical Name:formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester
CAS No.:255826-37-0
Molecular Formula:C₁₄H₂₁BrO₄Si
Molecular Weight:361.308
Hs Code.:

Synonyms:formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

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Chemical Property of formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

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Technology Process of formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

There total 4 articles about formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl 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: 96.0%

: 255826-36-9
3-bromo-4-{[(tert-butyl)(dimethyl)silyl]oxy}-5-methoxybenzaldehyde

: 255826-37-0
formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 2h; Heating;
DOI:10.1039/a901456j

Reference yield:

: 2973-76-4
5-bromo-4-hydroxy-3-methoxybenzaldehyde

: 255826-37-0
formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / imidazole / dimethylformamide / 4 h

2: 96 percent / m-chloroperbenzoic acid / CH₂Cl₂ / 2 h / Heating

With 1H-imidazole; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide; 1: Etherification / 2: Rearrangement;
DOI:10.1039/a901456j

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 255826-37-0
formic acid 4-(tert-butyldimethylsilanyloxy)-3-bromo-5-methoxyphenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / imidazole / dimethylformamide / 4 h

2: 96 percent / m-chloroperbenzoic acid / CH₂Cl₂ / 2 h / Heating

With 1H-imidazole; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide; 1: Etherification / 2: Rearrangement;
DOI:10.1039/a901456j