(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane

(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Suppliers list
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Shanghai YuYuan Pharmaceutical Co., Ltd.  
Tel: 13052276172
Email: product@yuyuanpharm.com
Company Name: Shanghai HuanChuan Industry Co.,Ltd.  
Tel: 021-61478794
Email: sales@hcshhai.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Hangzhou Molcore Biopharmatech Co.,Ltd  
Tel: 400-711-5280 86-571-81025280
Email: sales@molcore.com
(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Basic information
Product Name:(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane
Synonyms:(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane;Benzene, 2-bromo-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-methyl-
CAS:164513-48-8
MF:C13H21BrOSi
MW:301.29
EINECS:
Product Categories:
Mol File:164513-48-8.mol
(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Structure
(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Chemical Properties
Boiling point 293.6±28.0 °C(Predicted)
density 1.140±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Safety Information
MSDS Information
(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Usage And Synthesis
Synthesis
3-BROMO-4-METHYLPHENOL

60710-39-6

tert-Butyldimethylsilyl chloride

18162-48-6

(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane

164513-48-8

Step 1: To a solution of 3-bromo-4-methylphenol (0.20 g) in dichloromethane (3 mL) cooled in an ice bath, tert-butyldimethylsilyl chloride (0.18 g) and triethylamine (0.23 mL) were added. Subsequently, 4-dimethylaminopyridine (13 mg) was added and the reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, it was diluted with the addition of dichloromethane and the organic layer was washed sequentially with 1 M hydrochloric acid, aqueous NaHCO3 and brine and then dried with anhydrous MgSO4. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: cyclohexane/ethyl acetate) to give (3-bromo-4-methylphenoxy)(tert-butyl)dimethylsilane. Yield: 0.25 g (78% theoretical yield); LC (Method 1): tR = 1.59 min.

References[1] Patent: WO2012/72691, 2012, A1. Location in patent: Page/Page column 107-108
[2] Patent: US2012/302566, 2012, A1. Location in patent: Page/Page column 48
[3] Organic Letters, 2012, vol. 14, # 9, p. 2350 - 2353
(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane Preparation Products And Raw materials
Raw materials3-Bromo-4-methylphenol-->tert-Butyldimethylsilyl chloride-->Triethylamine-->Dichloromethane
Tag:(3-BroMo-4-Methylphenoxy)(tert-butyl)diMethylsilane(164513-48-8) Related Product Information
1-Bromo-3-(tert-butyldimethylsiloxy)benzene (4-Bromophenoxy)-tert-butyldimethylsilane Benzene, 1-bromo-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl- Benzene, 2-bromo-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,3-dimethyl- (3-bromo-4-fluorophenoxy)(tert-butyl)dimethylsilane Benzonitrile, 2-bromo-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-