BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER
BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER Basic information
- Product Name:
- BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER
- Synonyms:
-
- Methyl 2-methyl-4-bromobenzoate
- 4-BroMo-2-Methyl-benzoic acid Methyl ester
- BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER
- 2- Methyl-4-broMo benzoic acidMethyl ester
- 4-BROMO-2-METHYL-,METHYL ESTER
- CAS:
- 99548-55-7
- MF:
- C9H9BrO2
- MW:
- 229.07
- Mol File:
- 99548-55-7.mol
BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER Chemical Properties
- Melting point:
- 9 °C
- Boiling point:
- 273.6±20.0 °C(Predicted)
- Density
- 1.433±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- Appearance
- Colorless to light yellow Liquid
- InChI
- InChI=1S/C9H9BrO2/c1-6-5-7(10)3-4-8(6)9(11)12-2/h3-5H,1-2H3
- InChIKey
- CYEXEOXALMJXDI-UHFFFAOYSA-N
- SMILES
- C(OC)(=O)C1=CC=C(Br)C=C1C
BENZOIC ACID,4-BROMO-2-METHYL-,METHYL ESTER Usage And Synthesis
Chemical Properties
off-white powder
Uses
Methyl 4-Bromo-2-methylbenzoate can be used as an organic synthesis intermediate and a pharmaceutical intermediate.
Synthesis
68837-59-2
18107-18-1
99548-55-7
Step 1: To a mixed solution of 4-bromo-2-methylbenzoic acid (15.1 g, 0.070 mol) in tetrahydrofuran (180 mL) and methanol (45 mL) was slowly added dropwise (trimethylsilyl) diazomethane in 2.0 M hexane solution (42 mL, 0.084 mol) at 0 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure to afford methyl 4-bromo-2-methylbenzoate (16 g, 100% yield) as a yellow oil. The crude product could be used in the subsequent reaction without further purification. The product was characterized as follows: 1H NMR (400 MHz, CDCl3): δ 7.78 (d, 1H), 7.42 (s, 1H), 7.38 (d, 1H), 3.88 (s, 3H), 2.58 (s, 3H). Mass spectrum (EI): m/z 230 ([M+H]+, C9H9BrO2).
References
[1] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 4, p. 999 - 1004
[2] Patent: WO2009/55077, 2009, A1. Location in patent: Page/Page column 430
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 6, p. 2334 - 2356
[4] Patent: US2009/69370, 2009, A1. Location in patent: Page/Page column 17-18
[5] Patent: WO2009/158369, 2009, A1. Location in patent: Page/Page column 38; 39
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