ChemicalBook > Product Catalog >Organic Chemistry >Organic fluorine compound >Fluoro-benzoic acid series >METHYL 3-BROMO-5-FLUOROBENZOATE

METHYL 3-BROMO-5-FLUOROBENZOATE

METHYL 3-BROMO-5-FLUOROBENZOATE Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Beijing Ouhe Technology Co., Ltd  
Tel: 13552068683 13522913783
Email: 2355560935@qq.com
Company Name: Wuhan Haizheng Industry & Trade Development Co. Ltd  
Tel: 027-8866 0053/88660577/88660578
Email:

METHYL 3-BROMO-5-FLUOROBENZOATE manufacturers

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
Tag:METHYL 3-BROMO-5-FLUOROBENZOATE(334792-52-8) Related Product Information
Methyl dihydrojasmonate Methyl2-bromo-4-fluorobenzoate98%,Methyl 2-bromo-4-fluorobenzoate 98%,METHYL 2-BROMO-4-FLUOROBENZOATE Methyl 3-bromo-2-fluorobenzoate Methyl 4-bromo-2-fluorobenzoate METHYL 4-BROMO-3-FLUOROBENZOATE Methyl 3-bromo-4-fluorobenzoate 98%,Methyl3-bromo-4-fluorobenzoate98%,METHYL 3-BROMO-4-FLUOROBENZOATE METHYL 4-BROMO-3-FLUOROBENZOATE 98,Methyl 4-bromo-3-fluorobenzoate 98% Methyl2-bromo-5-fluorobenzoate98%,Methyl 2-bromo-5-fluorobenzoate 98%,METHYL 2-BROMO-5-FLUOROBENZOATE 3-BROMO-5-FLUOROBENZOIC ACID ETHYL ESTER RARECHEM AL BI 1432 3-Bromo-5-fluorobenzoic acid 3-BROMO-5-FLUOROBENZYL ALCOHOL 3-BROMO-5-FLUOROBENZALDEHYDE RARECHEM AL BF 1432 METHYL 3-BROMO-5-FLUOROBENZOATE