ChemicalBook--->CAS DataBase List--->99548-54-6

99548-54-6

99548-54-6 Structure

99548-54-6 Structure
IdentificationBack Directory
[Name]

3-BROMO-2-METHYL-BENZOIC ACID METHYL ESTER
[CAS]

99548-54-6
[Synonyms]

Methyl 3-Bromo-o-toluate
METHYL 3-BROMO-2-METHYLBENZOATE
3-BroMo-o-toluic Acid Methyl Ester
Methyl 3-bromo-2-methylbenzoate 97%
3-BroMo-2-Methyl-benzoic acid Methy
3-BROMO-2-METHYL-BENZOIC ACID METHYL ESTER
Benzoic acid, 3-broMo-2-Methyl-, Methyl ester
Methyl 3-bromo-o-toluate, 2-Bromo-6-(methoxycarbonyl)toluene
[Molecular Formula]

C9H9BrO2
[MDL Number]

MFCD09031772
[MOL File]

99548-54-6.mol
[Molecular Weight]

229.071
Chemical PropertiesBack Directory
[Melting point ]

29 °C
[Boiling point ]

140°C/21mmHg(lit.)
[density ]

1.433±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Chloroform
[form ]

Solid
[color ]

White
[InChI]

InChI=1S/C9H9BrO2/c1-6-7(9(11)12-2)4-3-5-8(6)10/h3-5H,1-2H3
[InChIKey]

MKQQTCSBXHAYQL-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC=CC(Br)=C1C
Questions And AnswerBack Directory
[Uses]

3-Bromo-2-methylbenzoic Acid Methyl Ester is a compound useful in organic synthesis.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[HS Code ]

2916399090
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Synthesis]

3-Bromo-2-methylbenzoic acid

76006-33-2

Iodomethane

74-88-4

3-BROMO-2-METHYL-BENZOIC ACID METHYL ESTER

99548-54-6

3-Bromo-2-methylbenzoic acid (16 g, 74.4 mmol) and iodomethane (21.2 g, 148.8 mmol) were reacted in DMF (160 mL) in the presence of sodium bicarbonate (12.5 g, 148.8 mmol). The reaction mixture was heated and stirred at 60 °C for 2 hours. After the reaction was completed, the mixture was cooled to room temperature and slowly poured into ice water (400 mL). The aqueous phase was extracted with ethyl acetate (4 x 100 mL) and the organic phases were combined. The organic phase was washed sequentially with water (3 x 100 mL) and saturated saline (100 mL) and then dried with anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure to give methyl 3-bromo-2-methylbenzoate (17.6 g, 100% yield) as an oil. The product was characterized by 1H NMR (CDCl3): δ 7.70 (t, J = 7.6 Hz, 2H), 7.08 (t, J = 7.9 Hz, 1H), 3.90 (s, 3H), 2.67 (s, 3H).

[References]

[1] Patent: US2003/96841, 2003, A1
[2] Patent: US2014/179667, 2014, A1. Location in patent: Paragraph 0802; 0803
[3] Patent: WO2008/65199, 2008, A1. Location in patent: Page/Page column 74
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-2-METHYL-BENZOIC ACID METHYL ESTER(99548-54-6)1HNMR
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