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(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate

Product Name
(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate
CAS No.
171230-81-2
Chemical Name
(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate
Synonyms
(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate;Methyl (R)-2-[(tert-Butyldimethylsilyl)oxy]propanoate;methyl (2R)-2-[tert-butyl(dimethyl)silyl]oxypropanoate;(R)-2-(tert-Butyl-dimethyl-silanyloxy)-propionic acid methyl ester;Propanoic acid, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl ester, (2R)-
CBNumber
CB53313490
Molecular Formula
C10H22O3Si
Formula Weight
218.37
MOL File
171230-81-2.mol
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(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate Property

Boiling point:
211.4±23.0 °C(Predicted)
Density 
0.911±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
M343173
Product name
(R)-Methyl2-((tert-butyldimethylsilyl)oxy)propanoate
Packaging
100mg
Price
$240
Updated
2021/12/16
AK Scientific
Product number
0830CS
Product name
(R)-Methyl2-((tert-butyldimethylsilyl)oxy)propanoate
Packaging
100mg
Price
$103
Updated
2021/12/16
AK Scientific
Product number
0830CS
Product name
(R)-Methyl2-((tert-butyldimethylsilyl)oxy)propanoate
Packaging
5g
Price
$551
Updated
2021/12/16
Ambeed
Product number
A155826
Product name
(R)-Methyl2-((tert-butyldimethylsilyl)oxy)propanoate
Purity
97%
Packaging
100mg
Price
$33
Updated
2021/12/16
Ambeed
Product number
A155826
Product name
(R)-Methyl2-((tert-butyldimethylsilyl)oxy)propanoate
Purity
97%
Packaging
250mg
Price
$59
Updated
2021/12/16
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(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate Chemical Properties,Usage,Production

Synthesis

17392-83-5

18162-48-6

171230-81-2

GENERAL STEPS: A mixture of methyl D-lactate (5.1 g, 48.99 mmol), dichloromethane (50 mL), imidazole (5 g, 75 mmol), and tert-butyldimethylchlorosilane (8.85 g, 58.79 mmol) was stirred for 2 hours at room temperature. After completion of the reaction, the mixture was diluted with water and extracted three times with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by medium pressure liquid chromatography (MPLC), using a petroleum ether solution of 5% ethyl acetate as eluent, to afford methyl (R)-2-((tert-butyldimethylsilyl)oxy)propionate (10.67 g, 100% yield) as a colorless oil.

References

[1] Patent: WO2015/171610, 2015, A2. Location in patent: Paragraph 000507
[2] Chemical Communications, 1997, # 13, p. 1219 - 1220
[3] Patent: WO2016/154533, 2016, A1. Location in patent: Paragraph 00176
[4] Tetrahedron Asymmetry, 2012, vol. 23, # 2, p. 117 - 123
[5] European Journal of Organic Chemistry, 2013, # 3, p. 525 - 532

(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate Preparation Products And Raw materials

Raw materials

Preparation Products

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(R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate Suppliers

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171230-81-2, (R)-methyl 2-(tert-butyldimethylsilyloxy)propanoateRelated Search:


  • (R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate
  • Propanoic acid, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl ester, (2R)-
  • (R)-2-(tert-Butyl-dimethyl-silanyloxy)-propionic acid methyl ester
  • methyl (2R)-2-[tert-butyl(dimethyl)silyl]oxypropanoate
  • Methyl (R)-2-[(tert-Butyldimethylsilyl)oxy]propanoate
  • 171230-81-2