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METHYL 3-BROMO-5-FLUOROBENZOATE

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CAS:334792-52-8
Purity:NLT 98% Package:1G;1KG;100KG
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CAS:334792-52-8
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CAS:334792-52-8
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CAS:334792-52-8
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Products Intro: Product Name:methyl 3-bromo-5-fluorobenzoate
CAS:334792-52-8

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METHYL 3-BROMO-5-FLUOROBENZOATE Basic information
Product Name:METHYL 3-BROMO-5-FLUOROBENZOATE
Synonyms:METHYL 3-BROMO-5-FLUOROBENZOATE;3-bromo-5-fluorobenzoate;Benzoic acid, 3-bromo-5-fluoro-, methyl ester
CAS:334792-52-8
MF:C8H6BrFO2
MW:233.03
EINECS:
Product Categories:Acids & Esters;Bromine Compounds;Fluorine Compounds
Mol File:334792-52-8.mol
METHYL 3-BROMO-5-FLUOROBENZOATE Structure
METHYL 3-BROMO-5-FLUOROBENZOATE Chemical Properties
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. Sealed in dry,Room Temperature
AppearanceColorless to light yellow Solid-Liquid Mixture
Safety Information
Hazard Codes T
Risk Statements 25-36
Safety Statements 26-45
RIDADR UN2810
HS Code 2914390090
MSDS Information
METHYL 3-BROMO-5-FLUOROBENZOATE Usage And Synthesis
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
METHYL 3-BROMO-5-FLUOROBENZOATE Preparation Products And Raw materials
Raw materials3-Bromo-5-fluorobenzoic acid-->Sodium bicarbonate-->Methanol-->3-Bromo-5-fluorobenzoyl chloride-->(TRIMETHYLSILYL)DIAZOMETHANE-->Sulfuric acid-->Diethyl ether
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