Identification | Back Directory | [Name]
4-methoxybutyric acid | [CAS]
29006-02-8 | [Synonyms]
m-PEG1-CH2-acid Einecs 249-366-5 m-PEG1-(CH2)3-acid 4-methoxybutanoicaci 4-methoxybutyric acid 4-Methoxybutanoic acid Butanoic acid, 4-methoxy- | [EINECS(EC#)]
249-366-5 | [Molecular Formula]
C5H10O3 | [MDL Number]
MFCD00029855 | [MOL File]
29006-02-8.mol | [Molecular Weight]
118.13 |
Chemical Properties | Back Directory | [Boiling point ]
146-147 °C(Press: 767 Torr) | [density ]
1.0057 g/cm3 | [storage temp. ]
Store at room temperature | [form ]
liquid | [pka]
4.63±0.10(Predicted) | [color ]
Colourless to light yellow |
Hazard Information | Back Directory | [Synthesis]
Example 25: Methyl 4-methoxybutyrate (1.0 g, 7.57 mmol) was dissolved in tetrahydrofuran (THF, 20 mL), and a solution of lithium hydroxide (LiOH, 0.362 g, 15.13 mmol) in water (H2O, 5 mL) was added. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the mixture was concentrated to dryness, acidified with 2 M hydrochloric acid (HCl), diluted with water (H2O), and extracted with ethyl acetate (EtOAc, 2×). The organic phases were combined, washed with saturated saline (brine), dried over anhydrous sodium sulfate (Na2SO4), and concentrated to dryness to give 4-methoxybutyric acid (860 mg, 96%) as a viscous oil.1H NMR (400 MHz, DMSO-d6): δ 12.02 (s, 1H), 3.28 (t, J=6.4 Hz, 2H), 3.19 (s, 3H ), 2.21 (t, J=7.4Hz, 2H), 1.69 (m, 2H). | [References]
[1] Patent: US2014/275080, 2014, A1. Location in patent: Paragraph 0446 [2] Patent: US2006/264489, 2006, A1. Location in patent: Page/Page column 87 [3] Patent: US2007/49603, 2007, A1. Location in patent: Page/Page column 90 [4] Patent: WO2009/50204, 2009, A1. Location in patent: Page/Page column 62 [5] Patent: WO2015/180612, 2015, A1. Location in patent: Page/Page column 52 |
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