METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE
METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE Basic information
- Product Name:
- METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE
- Synonyms:
-
- METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE
- 3-Bromo-5-bromomethyl-benzoic acid methyl ester
- Benzoic acid, 3-bromo-5-(bromomethyl)-, methyl ester
- CAS:
- 877624-40-3
- MF:
- C9H8Br2O2
- MW:
- 307.97
- Mol File:
- 877624-40-3.mol
METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE Chemical Properties
- Boiling point:
- 344.6±32.0 °C(Predicted)
- Density
- 1.780±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- White to light yellow Solid
METHYL 3-BROMO-5-(BROMOMETHYL)BENZOATE Usage And Synthesis
Synthesis
307353-32-8
877624-40-3
General procedure for the synthesis of methyl 3-bromo-5-(bromomethyl)benzoate from methyl 3-bromo-5-(hydroxymethyl)benzoate: methyl 3-bromo-5-(hydroxymethyl)benzoate (2.0 g, 8.2 mmol) was mixed with triphenylphosphine (4.28 g, 16.3 mmol) in tetrahydrofuran (20 mL) and the mixture was cooled down to 0°C. The reaction was completed by the addition of N-bromosuccinimidamide (3.05 g, 17.1 mmol). Subsequently, N-bromosuccinimide (3.05 g, 17.1 mmol) was added in batches and the reaction mixture was allowed to gradually warm up to room temperature. After 16 h of reaction, the reaction mixture was diluted with ethyl acetate, washed sequentially with saturated sodium bicarbonate solution (2×) and brine (2×), the organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure. Purification by silica gel column chromatography (eluent: 10% ethyl acetate/hexane) gave 2.1 g of light brown oily product in 83% yield. The product was identified by 1H-NMR (CDCl3, 300 MHz): δ 8.07 (s, 1H), 7.96 (s, 1H), 7.70 (s, 1H), 4.42 (s, 2H), 3.90 (s, 3H). Mass spectrometry analysis showed a molecular ion peak of 308.93 (MH)+.
References
[1] Patent: US2007/249607, 2007, A1. Location in patent: Page/Page column 85
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