Basic information Safety Supplier Related

TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE

Basic information Safety Supplier Related

TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE Basic information

Product Name:
TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE
Synonyms:
  • TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE
  • (1,1-DIMETHYLETHYL)(2-IODOETHOXY)DIMETHYL-SILANE
  • 1-(tert-Butyldimethylsilyloxy)-2-iodoethane
  • 1-Iodo-2-(tert-butyldimethylsilyloxy)ethane
  • 2-Iodo-1-(1,1,2,2-tetramethyl-1-silapropoxy)ethane
  • Silane,(1,1-dimethylethyl)(2-iodoethoxy)dimethyl-
  • tert-Butyl(2-iodoethoxy)
  • DK442
CAS:
101166-65-8
MF:
C8H19IOSi
MW:
286.23
Mol File:
101166-65-8.mol
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TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE Chemical Properties

Boiling point:
210℃
Density 
1.291
refractive index 
1.48
Flash point:
81℃
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
clear liquid
color 
Colorless to Yellow to Orange
InChI
InChI=1S/C8H19IOSi/c1-8(2,3)11(4,5)10-7-6-9/h6-7H2,1-5H3
InChIKey
CAAUZMMMFDVBFD-UHFFFAOYSA-N
SMILES
[Si](C(C)(C)C)(OCCI)(C)C
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Safety Information

HS Code 
2931.90.9010
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TERT-BUTYL-(2-IODO-ETHOXY)-DIMETHYL-SILANE Usage And Synthesis

Synthesis

624-76-0

18162-48-6

101166-65-8

(i) Preparation of tert-butyl-(2-iodoethoxy)dimethylsilane To a stirred solution of 2-iodoethanol (17.2 g, 100 mmol) and imidazole (8.17 g, 120 mmol) in dichloromethane (100 mL) was slowly added tert-butyldimethylmethylsilyl chloride (15.83 g, 105 mmol) at a controlled rate of addition to maintain the reaction temperature at no more than 30 °C. The reaction was carried out by stirring the mixture for 17 hours. After addition, the reaction mixture was continued to be stirred for 17 hours. Upon completion of the reaction, the organic phase was washed sequentially with water (2 x 50 mL) and brine (50 mL), followed by drying with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the colorless liquid-like product tert-butyl-(2-iodoethoxy)dimethylsilane (28.0 g, 97.8 mmol, 98% yield). 1H-NMR (400 MHz, CDCl3): δ = 3.83 (t, 2H, J = 7.0 Hz), 3.20 (t, 2H, J = 7.0 Hz), 0.90 (s, 9H), 0.08 (s, 6H) ppm.

References

[1] Chemistry - A European Journal, 2017, vol. 23, # 5, p. 1157 - 1165
[2] Analytical Chemistry, 2003, vol. 75, # 21, p. 6002 - 6010
[3] Patent: US2013/59970, 2013, A1. Location in patent: Paragraph 0311; 0312; 0313
[4] Patent: US2014/249162, 2014, A1. Location in patent: Paragraph 0234
[5] Patent: EP2781519, 2014, A1. Location in patent: Paragraph 0232

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