ChemicalBook--->CAS DataBase List--->4324-37-2

4324-37-2

4324-37-2 Structure

4324-37-2 Structure
IdentificationBack Directory
[Name]

2-methoxypropionic acid
[CAS]

4324-37-2
[Synonyms]

Einecs 224-356-3
2-methoxypropionic acid
2-methoxypropanoic acid
Propanoic acid, 2-methoxy-
alpha-Methoxypropionic acid
2-methoxypropanoic acid(SALTDATA: FREE)
[EINECS(EC#)]

224-356-3
[Molecular Formula]

C4H8O3
[MDL Number]

MFCD00126928
[MOL File]

4324-37-2.mol
[Molecular Weight]

104.105
Chemical PropertiesBack Directory
[Melting point ]

128.5 °C
[Boiling point ]

199℃
[density ]

1.085
[Fp ]

87℃
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[pka]

3.59±0.10(Predicted)
[color ]

Colorless
[InChI]

InChI=1S/C4H8O3/c1-3(7-2)4(5)6/h3H,1-2H3,(H,5,6)
[InChIKey]

ICPWFHKNYYRBSZ-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C(OC)C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335-H302
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

2-methoxypropionic acid(4324-37-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Sodium Methoxide

124-41-4

2-Bromopropionic acid

598-72-1

2-methoxypropionic acid

4324-37-2

A methanolic solution of 25% sodium methanolate (16 mL) was slowly added dropwise to a stirring solution of 2-bromopropionic acid (19.6 mmol) in methanol (5 mL) under nitrogen protection. The reaction mixture was heated and reacted at 50 °C overnight while continuously protected by the passage of nitrogen. Upon completion of the reaction, the reaction solution was concentrated under reduced pressure by rotary evaporator. The residue was adjusted to pH 1 with aqueous 1N hydrochloric acid, followed by three extractions with ethyl acetate (70 mL, 25 mL, 10 mL). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated again under reduced pressure to afford 2-methoxypropionic acid as a colorless oil in the yield of 2.04 g (99% yield), which was pure enough to be used directly in the subsequent reaction without further purification. The product was characterized by 1H NMR (CD3OD): δ 3.67 (q, 1H), 3.33 (s, 3H), 1.33 ppm (d, 3H).

[References]

[1] Patent: WO2006/96338, 2006, A1. Location in patent: Page/Page column 41
[2] Patent: WO2006/133006, 2006, A2. Location in patent: Page/Page column 46-47
[3] Australian Journal of Chemistry, 1980, vol. 33, # 4, p. 809 - 821
[4] Organic Letters, 2018, vol. 20, # 16, p. 4867 - 4870
[5] Patent: KR2015/128789, 2015, A. Location in patent: Paragraph 0896; 0898; 0899
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