
Methyl 2-bromobenzoate synthesis
- Product Name:Methyl 2-bromobenzoate
- CAS Number:610-94-6
- Molecular formula:C8H7BrO2
- Molecular Weight:215.04

88-65-3
349 suppliers
$5.00/5g

119-36-8
1020 suppliers
$5.00/10g

610-94-6
309 suppliers
$13.00/25g

69-72-7
1290 suppliers
$5.00/10g
Yield:610-94-6 91%
Reaction Conditions:
Stage #1:2-bromobenzoic-acid with potassium carbonate in N,N-dimethyl acetamide at 110; for 0.5 h;
Stage #2:methyl salicylate at 110; for 24 h;
Steps:
Methyl 2-Methoxybenzoate (3a); Typical Procedure
General procedure: A mixture of 2-methoxybenzoic acid (3.8 g, 25 mmol) and K2CO3 (2.07 g, 15 mmol) in DMA (50 mL) was stirred at 110 °C for 0.5 h. Methyl salicylate (5.70 g, 37.5 mmol) was added and the resulting mixture was stirred for 24 h. The solvent was then removed in vacuo. After cooling to r.t., K2CO3 (2.42 g, 17.5 mmol) and water (50mL) were added to hydrolyze the excess methyl salicylate. The resulting mixture was heated at 60 °C until methyl salicylate disappeared on TLC. Then, the solution was extracted with EtOAc (3 ×20 mL). The organic layer was washed with water, sat. aq NaCl solution,and dried (anhyd MgSO4). Evaporation of solvent in vacuoafforded methyl 2-methoxybenzoate (3.82 g, 92%). More than 90% of salicylic acid was recovered as a white precipitate by acidifying the aqueous phase with 1 M HCl.
References:
Chen, Si;Jia, Lei;Li, Xiaonan;Luo, Meiming [Synthesis,2014,vol. 46,# 2,art. no. SS-2013-H0569-OP,p. 263 - 268]

75-91-2
203 suppliers
$26.00/100g

95-46-5
307 suppliers
$10.00/10 g

610-94-6
309 suppliers
$13.00/25g

93-58-3
504 suppliers
$13.50/100 mL

610-94-6
309 suppliers
$13.00/25g

75-91-2
203 suppliers
$26.00/100g

6630-33-7
426 suppliers
$9.00/10g

610-94-6
309 suppliers
$13.00/25g