ChemicalBook--->CAS DataBase List--->334792-52-8

334792-52-8

334792-52-8 Structure

334792-52-8 Structure
IdentificationBack Directory
[Name]

METHYL 3-BROMO-5-FLUOROBENZOATE
[CAS]

334792-52-8
[Synonyms]

3-bromo-5-fluorobenzoate
METHYL 3-BROMO-5-FLUOROBENZOATE
Benzoic acid, 3-bromo-5-fluoro-, methyl ester
[Molecular Formula]

C8H6BrFO2
[MDL Number]

MFCD07780735
[MOL File]

334792-52-8.mol
[Molecular Weight]

233.03
Chemical PropertiesBack Directory
[Boiling point ]

251.6±25.0℃ (760 Torr)
[density ]

1.577±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

106.0±23.2℃
[refractive index ]

1.5345
[storage temp. ]

Room temperature.
[Appearance]

Colorless to light yellow Solid-Liquid Mixture
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362+P364-P403+P233-P501c
[Hazard Codes ]

T
[Risk Statements ]

25-36
[Safety Statements ]

26-45
[RIDADR ]

UN2810
[HS Code ]

2914390090
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 3-BROMO-5-FLUOROBENZOATE(334792-52-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Bromo-5-fluorobenzoic acid

176548-70-2

Sodium bicarbonate

144-55-8

METHYL 3-BROMO-5-FLUOROBENZOATE

334792-52-8

The general procedure for the synthesis of methyl 3-bromo-5-fluorobenzoate from 3-bromo-5-fluorobenzoic acid and sodium bicarbonate is as follows: 1. Preparation of intermediate 25: methyl 3-bromo-5-fluorobenzoate - A solution was prepared by dissolving 3-bromo-5-fluorobenzoic acid (3.1 g, 14 mmol) in methanol (30 ml). - Concentrated sulfuric acid (3.0 ml) was slowly added to the above solution. - The reaction mixture was heated to reflux and maintained for 1.5 hours. - After completion of the reaction, the mixture was cooled to room temperature. - The cooled reaction mixture was neutralized by slowly pouring it into 400 ml of saturated aqueous sodium bicarbonate solution. - The aqueous phase was extracted twice with diethyl ether (250 ml) and the organic layers were combined. - The organic layer was dried with anhydrous magnesium sulfate and subsequently concentrated under reduced pressure to afford the target product methyl 3-bromo-5-fluorobenzoate (2.6 g, 80% yield). The physicochemical properties of the intermediate 25 need to be further determined or obtained by consulting the relevant literature.

[References]

[1] Patent: EP1229024, 2002, A1
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