2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER
- Product Name
- 2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER
- CAS No.
- 788081-99-2
- Chemical Name
- 2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER
- Synonyms
- Methyl 2-(broMoMethyl)-5-Methoxybenzoate;2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER;Benzoic acid, 2-(bromomethyl)-5-methoxy-, methyl ester
- CBNumber
- CB52460827
- Molecular Formula
- C10H11BrO3
- Formula Weight
- 259.1
- MOL File
- 788081-99-2.mol
2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER Property
- Boiling point:
- 342.5±32.0 °C(Predicted)
- Density
- 1.432±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
N-Bromosuccinimide Price
- Product number
- 2336AC
- Product name
- Methyl2-(bromomethyl)-5-methoxybenzoate
- Packaging
- 25g
- Price
- $691
- Updated
- 2021/12/16
- Product number
- HCH0030254
- Product name
- BENZOIC ACID, 2-(BROMOMETHYL)-5-METHOXY-, METHYL ESTER
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $1089.05
- Updated
- 2021/12/16
- Product number
- 2336AC
- Product name
- Methyl2-(bromomethyl)-5-methoxybenzoate
- Packaging
- 100g
- Price
- $2051
- Updated
- 2021/12/16
- Product number
- HCH0030254
- Product name
- BENZOIC ACID, 2-(BROMOMETHYL)-5-METHOXY-, METHYL ESTER
- Purity
- 95.00%
- Packaging
- 5G
- Price
- $2233.89
- Updated
- 2021/12/16
- Product number
- CD12030904
- Product name
- Methyl2-(bromomethyl)-5-methoxybenzoate
- Purity
- 98%
- Packaging
- 25g
- Price
- $2075
- Updated
- 2021/12/16
2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER Chemical Properties,Usage,Production
Synthesis
73502-03-1
788081-99-2
General procedure for the synthesis of methyl 2-bromomethyl-5-methoxybenzoate from methyl 2-methyl-5-methoxybenzoate: Preparation of intermediate 12: Compound 11 (4.4 g, 24.2 mmol) was dissolved in carbon tetrachloride (80 mL) and N-bromosuccinimide (4.48 g, 24.2 mmol) and benzoyl peroxide (276 mg 1.13 mmol). The reaction mixture was heated to reflux and stirred for 3 hours. After completion of the reaction, the solid insoluble material was removed by filtration and the filter cake was washed with ether. The organic phases were combined, washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the target product 12 (6.1 g, 98% yield). Product characterization data: mass spectrum (LCMS) m/z 260 ([M+H]+), 1H NMR (CDCl3) δ 4.50 (2H, s, CH2Br), 3.73 (3H, s, OCH3), 3.88 (3H, s, CO2CH3), 6.86-7.50 (m, 3H, Ar-H).
References
[1] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 17, p. 5286 - 5289
[2] Patent: WO2009/14637, 2009, A2. Location in patent: Page/Page column 70
[3] Patent: WO2010/54279, 2010, A1. Location in patent: Page/Page column 100
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 24, p. 7283 - 7287
[5] Patent: WO2006/138549, 2006, A1. Location in patent: Page/Page column 73
2-BROMOMETHYL-5-METHOXY-BENZOIC ACID METHYL ESTER Preparation Products And Raw materials
Raw materials
Preparation Products
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