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Chemical Structure| 2100306-80-5 Chemical Structure| 2100306-80-5

Structure of Hydroxy-peg5-methyl ester
CAS No.: 2100306-80-5

Chemical Structure| 2100306-80-5

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Product Details of [ 2100306-80-5 ]

CAS No. :2100306-80-5
Formula : C14H28O8
M.W : 324.37
SMILES Code : COC(CCOCCOCCOCCOCCOCCO)=O
English Name :Hydroxy-peg5-methyl ester
MDL No. :MFCD30730370

Safety of [ 2100306-80-5 ]

Application In Synthesis of [ 2100306-80-5 ]

* 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 [ 2100306-80-5 ]

[ 2100306-80-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2100306-80-5 ]
  • [ 98-59-9 ]
  • [ 2802468-55-7 ]
YieldReaction ConditionsOperation in experiment
43% With triethylamine In tetrahydrofuran at 25℃; for 10h; 29 Synthesis of methyl l-(tosyloxy)-3, 6, 9, 12, 15-pentaoxaoctadecan-18-oate To a solution of methyl 3-[2-[2-[2-[2-(2-hydroxy ethoxy)ethoxy] ethoxy] ethoxy] ethoxy] propanoate (550 mg, 1.70 mmol,) in THF (2.5 mL) was added triethylamine (343 mg, 3.39 mmol) at 25 °C. A solution of 4-methylbenzenesulfonyl chloride (356 mg, 1.87 mmol) in THF (2.5 mL) was added and the mixture stirred at 25 °C for 10 h. The solvent was removed in vacuo, and the residue was purified by column chromatography (SiO2, dichloromethane/methanol 50:1 to 5:1) to give the title compound as a colourless oil. Yield 360 mg (43%). m/z: [ESI+] 479.0 (M+H)+, (C21H34O10S).
43% With triethylamine In tetrahydrofuran at 25℃; for 10h; 29 Synthesis of methyl l-(tosyloxy)-3, 6, 9, 12, 15-pentaoxaoctadecan-18-oate To a solution of methyl 3-[2-[2-[2-[2-(2-hydroxy ethoxy)ethoxy] ethoxy] ethoxy] ethoxy] propanoate (550 mg, 1.70 mmol,) in THF (2.5 mL) was added triethylamine (343 mg, 3.39 mmol) at 25 °C. A solution of 4-methylbenzenesulfonyl chloride (356 mg, 1.87 mmol) in THF (2.5 mL) was added and the mixture stirred at 25 °C for 10 h. The solvent was removed in vacuo, and the residue was purified by column chromatography (SiO2, dichloromethane/methanol 50:1 to 5:1) to give the title compound as a colourless oil. Yield 360 mg (43%). m/z: [ESI+] 479.0 (M+H)+, (C21H34O10S).
  • 2
  • [ 2100306-80-5 ]
  • [ 2802468-57-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran / 10 h / 25 °C 2: potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C
 

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