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Chemical Structure| 85475-01-0 Chemical Structure| 85475-01-0
Chemical Structure| 85475-01-0

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Hydroxy-PEG1-methylamine is a PEG derivative containing a hydroxyl group and a methylamine group. The hydrophilic PEG spacer enhances solubility in aqueous media, and the hydroxyl group enables further derivatization or replacement with other reactive groups. The methylamine group is reactive with carboxylic acids, carbonyls, and other functional groups.

4.5 *For Research Use Only !

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Product Details of Hydroxy-PEG1-methylamine

CAS No. :85475-01-0
Formula : C5H13NO2
M.W : 119.16
SMILES Code : CNCCOCCO
MDL No. :MFCD12783671

Safety of Hydroxy-PEG1-methylamine

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H335-H314-H227
Precautionary Statements:P210-P260-P264-P270-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P370+P378-P403+P233-P403+P235-P405-P501
Class:8
UN#:2735
Packing Group:

Application In Synthesis of Hydroxy-PEG1-methylamine

* 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 [ 85475-01-0 ]

[ 85475-01-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 593-51-1 ]
  • [ 118591-58-5 ]
  • [ 85475-01-0 ]
YieldReaction ConditionsOperation in experiment
52% With potassium carbonate; In 1,4-dioxane; at 50℃; Compound 1-3 (5.1 g, 19.6 mmol) was dissolved in 1,4-dioxane (50 mL), followed by addition of methylamine hydrochloride 1-4 (13.4 g, 196 mmol), and potassium carbonate (13.8 g, 100 mmol) was added under stirring in batches, followed by stirring the reaction overnight under conditions of 50° C. and a closed reaction system, TLC monitoring showed that the starting material 1-3 was completely reacted. The solvent was removed under reduced pressure to obtain a concentrated residue. The concentrated residue was dispensed with dichloromethane (20 mL), an appropriate amount of silica gel was added and the sample was stirred, spin-dried under reduced pressure and directly placed on a silica gel column for column chromatographic purification, with an eluent (dichloromethane:methanol=20/1-5/1) to obtain the target product 1-5 (1.2 g, 52percent) as a pale yellow oil, LC-MS: m/z=120[M+H]+.
  • 2
  • [ 118591-58-5 ]
  • [ 74-89-5 ]
  • [ 85475-01-0 ]
YieldReaction ConditionsOperation in experiment
99% at 85℃; for 16h;Inert atmosphere; A mixture of 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (3 g, 11.52 mmol, 1 eq) in methanamine (11.93 g, 115.25 mmol, 10 eq) was degassed and purged with nitrogen for 3 times, and then the mixture was stirred at 85 C for 16 hours under nitrogen. The reaction mixture was concentrated under reduced pressure to give a residue. Compound 2-[2- (methylamino)ethoxy] ethanol (1.37 g, 11.50 mmol, 99% yield) was obtained as a yellow oil. 'H- NMR (400MHz, CDCb) d 3.72 - 3.47 (m, 8H), 2.67 - 2.63 (m, 3H).
at 70℃; for 12h;Sealed tube; A solution of 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (2.50 g, 9.60 mmol, 1 eq) and methanamine (40.0 mL, 1.00 eq) in sealed tube was stirred at 70 C. for 12 hours. Analysis by TLC indicated 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate was consumed completely. The reaction mixture was concentrated under reduced pressure to remove methanamine (40.0 mL, 1.00 eq) to give 2-[2-(methylamino)ethoxy]ethanol (1.10 g, crude) as a yellow oil.
 

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