ChemicalBook--->CAS DataBase List--->26825-95-6

26825-95-6

26825-95-6 Structure

26825-95-6 Structure
IdentificationBack Directory
[Name]

methyl 12-bromododecanoate
[CAS]

26825-95-6
[Synonyms]

methyl 12-bromododecanoate
12-bromo-dodecanoic acid methyl ester
Dodecanoic acid, 12-bromo-, methyl ester
[Molecular Formula]

C13H25BrO2
[MDL Number]

MFCD01838179
[MOL File]

26825-95-6.mol
[Molecular Weight]

293.24
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

liquid
[color ]

Clear, pale lemon
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P261
[HS Code ]

2915907098
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 12-bromododecanoate(26825-95-6)FT-IR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

12-Bromododecanoic acid

73367-80-3

methyl 12-bromododecanoate

26825-95-6

Under argon protection, 12-bromododecanoic acid (6) (1.0 g, 3.59 mmol) was dissolved in anhydrous methanol (10 mL) containing concentrated sulfuric acid (200 μL) and the reaction was heated to reflux for 15 hours. After completion of the reaction, methanol was removed by distillation under reduced pressure. The residue was diluted with ethyl acetate (100 mL), washed sequentially with saturated sodium bicarbonate solution (3×20 mL) and brine (2×20 mL), and the organic phase was dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure to obtain the crude product. Purification by silica gel column chromatography using petroleum ether/ethyl acetate (97.5:2.5) as eluent afforded the target product methyl 12-bromododecanoate (7) (974 mg, 3.32 mmol, 93% yield) as a colorless oil. The product was analyzed by thin-layer chromatography (TLC, Rf 0.45, petroleum ether/ethyl acetate, 9:1), infrared spectroscopy (IR), nuclear magnetic resonance hydrogen spectroscopy (1H NMR), nuclear magnetic resonance carbon spectroscopy (13C NMR) and high-resolution mass spectrometry (HRMS).

[References]

[1] Journal of Antibiotics, 1995, vol. 48, # 12, p. 1467 - 1480
[2] Journal of Heterocyclic Chemistry, 2001, vol. 38, # 6, p. 1393 - 1400
[3] Analytical Biochemistry, 2014, vol. 456, # 1, p. 70 - 81
[4] Patent: WO2017/49245, 2017, A2. Location in patent: Paragraph 00539-00540
[5] Patent: WO2017/112865, 2017, A1. Location in patent: Paragraph 00618
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