| Identification | Back Directory | [Name]
Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate) | [CAS]
77544-68-4 | [Synonyms]
PEG4-Tos
PEG3-Tos
77544-68-4
OH-PEG3-Tos
Tos-PEG3-OH
os-PEG3-alcohol
Hydroxy-PEG3-Tos
Tos-PEG4-alcohol
Tos-PEG3-alcohol
Triethylene glycol p-toluenesulfonate
2-(2-(2-Hydroxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonate
2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate)
Ethanol, 2-[2-(2-hydroxyethoxy)ethoxy]-, 1-(4-Methylbenzenesulfonate) | [Molecular Formula]
C13H20O6S | [MDL Number]
MFCD22574797 | [MOL File]
77544-68-4.mol | [Molecular Weight]
304.36 |
| Chemical Properties | Back Directory | [Boiling point ]
460.0±35.0 °C(Predicted) | [density ]
1.234±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
Ethanol: 100 mg/mL (328.56 mM); DMSO: 100 mg/mL (328.56 mM and warming) | [form ]
Solid-Liquid Mixture | [pka]
14.36±0.10(Predicted) | [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 |
| Hazard Information | Back Directory | [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 |
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