Basic information Safety Supplier Related

methyl 4-(bromomethyl)-2-methoxybenzoate

Basic information Safety Supplier Related

methyl 4-(bromomethyl)-2-methoxybenzoate Basic information

Product Name:
methyl 4-(bromomethyl)-2-methoxybenzoate
Synonyms:
  • methyl 4-(bromomethyl)-2-methoxybenzoate
  • 2-Methoxy-4-(broMoMethyl)benzoic acid Methyl ester
  • 4-broMoMethyl-2-Methoxy benzoic acid Methyl ester
  • Methyl 2-Methoxy-4-(bromomethyl)benzoate
  • Benzoic acid, 4-(bromomethyl)-2-methoxy-, methyl ester
  • )-2-methoxybenzoate
  • Oxirane, 2-[7-(phenylMethoxy)ethyl]-
CAS:
74733-27-0
MF:
C10H11BrO3
MW:
259.1
Mol File:
74733-27-0.mol
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methyl 4-(bromomethyl)-2-methoxybenzoate Chemical Properties

Boiling point:
142-146 °C(Press: 1.8 Torr)
Density 
1.432±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
InChI
InChI=1S/C10H11BrO3/c1-13-9-5-7(6-11)3-4-8(9)10(12)14-2/h3-5H,6H2,1-2H3
InChIKey
DCXFLSHDURQRML-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(CBr)C=C1OC
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methyl 4-(bromomethyl)-2-methoxybenzoate Usage And Synthesis

Synthesis

81245-24-1

74733-27-0

General procedure for the synthesis of methyl 4-bromomethyl-2-methoxybenzoate from methyl 2-methoxy-4-methylbenzoate: over a period of 1.5 h, bromine (6.19 mL, 120 mmol) was slowly added dropwise over a period of 1.5 h to a reflux mixture of methyl 2-methoxy-4-methylbenzoate (21.625 g, 120 mmol) in carbon tetrachloride (240 mL) dissolved in a carbon tetrachloride (75 mL). During the dropwise addition, the reaction mixture was irradiated using a 250W tungsten lamp. After dropwise addition, the reaction was continued at reflux for 15 minutes. Upon completion of the reaction, the mixture was concentrated and the solvent was removed under vacuum to afford methyl 4-bromomethyl-2-methoxybenzoate as an oily product (29.864 g, 96% yield). The product was confirmed by NMR hydrogen spectrum (400 MHz, CDCl3): δ 2.40 (s, 3H), 3.87 (s, 3H), 3.91 (s, 3H), 4.44 (s, 2H). Mass spectrometry (FIA-MS) showed the molecular ion peak m/e: 259 ([M+1]+).

References

[1] Patent: WO2004/108677, 2004, A1. Location in patent: Page 199
[2] Synlett, 2014, vol. 25, # 17, p. 2485 - 2487
[3] Patent: US2009/209586, 2009, A1. Location in patent: Page/Page column 13
[4] Patent: KR2016/20674, 2016, A. Location in patent: Paragraph 0053; 0115; 0116
[5] Bulletin de la Societe Chimique de France, 1962, p. 2255 - 2261

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