Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate) Chemical Properties

Boiling point:

460.0±35.0 °C(Predicted)

Density 

1.234±0.06 g/cm3(Predicted)

storage temp. 

under inert gas (nitrogen or Argon) at 2-8°C

solubility 

Ethanol: 100 mg/mL (328.56 mM); DMSO: 100 mg/mL (328.56 mM and warming)

pka

14.36±0.10(Predicted)

form 

Solid-Liquid Mixture

color 

Colorless to light yellow

Water Solubility 

Water: 10 mg/mL (32.86 mM)

InChI

InChI=1S/C13H20O6S/c1-12-2-4-13(5-3-12)20(15,16)19-11-10-18-9-8-17-7-6-14/h2-5,14H,6-11H2,1H3

InChIKey

RSUCRUOTLCQWFX-UHFFFAOYSA-N

SMILES

C(OS(C1=CC=C(C)C=C1)(=O)=O)COCCOCCO

Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate) Usage And Synthesis

Description

PEG3-Tos is a PEG linker containing a hydroxyl group and a tosyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The tosyl group is a very good leaving group for nucleophilic substitution reactions.

Uses

Tos-PEG3 is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Tos-PEG3 (structure 1) can be used for the synthesis of 3'-aminooxy oligonucleotides solid supports[1].

Synthesis

Triethylene glycol (16.81 g, 112 mmol) was dissolved in 20 mL of tetrahydrofuran (THF) and preconfigured aqueous sodium hydroxide solution (6.73 g, 168 mmol, dissolved in 15 mL of water) was added. After cooling the reaction mixture to 0°C in an ice water bath, a THF solution (150 mL) of p-toluenesulfonyl chloride (TsCl, 25.67 g, 135 mmol) was added slowly and dropwise. The reaction mixture was continued to be stirred at 0°C for 1 hour. Upon completion of the reaction, the solvent was removed by rotary evaporator. The residue was dissolved in dichloromethane (DCM) and washed sequentially with saturated saline (if there is too much salt in the organic phase, it can be washed with water first). After the organic phase was dried over anhydrous magnesium sulfate, the crude product was purified by column chromatography using hexane/ethyl acetate (2:1, v/v) as eluent to afford the yellow oily target product triethylene glycol mono-p-toluenesulfonate. Yield: 89%. 1H NMR (CDCl3) δ: 2.44 (s, 3H, CH3), 3.51-3.70 (m, 12H, 6×CH2), 7.34 (d, 2H, Ar-H), 7.80 (d, 2H, Ar-H). Mass spectrum (MALDI-TOF): m/z calculated value 304.1; measured value 327.21 [M+Na]+.

References

[1] No?l M, et al. Solid Supports for the Synthesis of 3'-Aminooxy Deoxy- or Ribo-oligonucleotides and Their 3'-Conjugation by Oxime Ligation.J Org Chem. 2019 Nov 15;84(22):14854-14860. DOI:10.1021/acs.joc.9b00848

Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate)(77544-68-4)Related Product Information

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