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Chemical Structure| 439114-12-2 Chemical Structure| 439114-12-2
Chemical Structure| 439114-12-2

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Synonyms: Bis-PEG6-t-butyl ester

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Product Details of Bis-PEG6-t-butyl ester

CAS No. :439114-12-2
Formula : C22H42O9
M.W : 450.56
SMILES Code : O=C(OC(C)(C)C)CCOCCOCCOCCOCCOCCC(OC(C)(C)C)=O
Synonyms :
Bis-PEG6-t-butyl ester
MDL No. :MFCD18916981

Safety of Bis-PEG6-t-butyl ester

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of Bis-PEG6-t-butyl ester

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 439114-12-2 ]

[ 439114-12-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 439114-12-2 ]
  • [ 76-05-1 ]
  • [ 439114-13-3 ]
YieldReaction ConditionsOperation in experiment
In hydrogenchloride; dichloromethane; b) 3-[2-(2-{2-[2-(2-Carboxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]propionic acid (40) A solution of tert-butyl 3-[2-(2-{2-[2-(2-tert-butoxycarbonylethoxy)ethoxy]ethoxy}-ethoxy)ethoxy]propionate 24 in 50 ml of methylene chloride and 50 ml of trifluoro-acetic acid is stirred for 2 h and then concentrated. The residue is taken up in 1N hydrochloric acid and extracted with methylene chloride. The organic phase is concentrated and contains 40. C14H26O9 (338.36) MS (ESI) 339 (M+H)
  • 2
  • [ 439114-12-2 ]
  • [ 439114-13-3 ]
YieldReaction ConditionsOperation in experiment
82% With methoxybenzene; trifluoroacetic acid; at 0 - 20℃; for 3h; A solution of 3-{2-[2-(2-{2-[2-(2-tert-Butoxycarbonyl-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl ester (6 g, 18.6 mmol) in anisole (20 ml) was cooled in an ice bath and trifluroacetic acid (65 g) was added. After 3 hrs at RT volatiles were removed under reduced pressure and the residue was partitioned between ethyl acetate (50 ml) and 5% sodium bicarbonate solution. The aqueous layer was acidified with 1 N HCl, saturated with NaCl and then extracted with ethyl acetate (3×50 ml). Combined organic layers were washed with brine and dried over sodium sulfate. Removal of volatiles under the reduced pressure provided the product as colorless liquid which solidified upon refrigeration (3.8 g, 82%).
82% A solution of 3-{2-[2-(2-{2-[2-(2-tert-Butoxycarbonyl-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl ester (6 g, 18.6 mmol) in anisole (20 ml) was cooled in an ice bath and trifluoroacetic acid (65 g) was added. After 3 hrs at RT volatiles were removed under reduced pressure and the residue was partitioned between ethyl acetate (50 ml) and 5% sodium bicarbonate solution. The aqueous layer was acidified with 1 N HCl, saturated with NaCl and then extracted with ethyl acetate (3*50 ml). Combined organic layers were washed with brine and dried over sodium sulfate. Removal of volatiles under the reduced pressure provided the product as colorless liquid which solidified upon refrigeration (3.8 g, 82%).
 

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