Dimethyl 4-bromophthalate

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Dimethyl 4-bromophthalate Basic information
Product Name:Dimethyl 4-bromophthalate
Synonyms:1,2-Benzenedicarboxylic acid, 4-broMo-, 1,2-diMethyl ester;Dimethyl 4-bromophthalate
CAS:87639-57-4
MF:C10H9BrO4
MW:273.08
EINECS:
Product Categories:
Mol File:87639-57-4.mol
Dimethyl 4-bromophthalate Structure
Dimethyl 4-bromophthalate Chemical Properties
Melting point 33-35 °C
Boiling point 177-178 °C(Press: 13 Torr)
density 1.505±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceWhite to yellow <38°C Solid,>40°C Liquid
Safety Information
HS Code 2917399590
MSDS Information
Dimethyl 4-bromophthalate Usage And Synthesis
Synthesis
4-BROMO PHTHALIC ANHYDRUS

86-90-8

DIMETHYL 4-BROMOPHTHALATE

87639-57-4

General procedure for the synthesis of dimethyl 4-bromophthalate using 5-bromoisobenzofuran-1,3-dione as starting material:(15-1) Synthesis of dimethyl 4-bromophthalate. Methanol (500 mL) was added to 4-bromophthalic anhydride (50.25 g). Subsequently, chlorosulfonic acid (1 mL) was added dropwise to the reaction system. The resulting reaction mixture was heated under reflux conditions overnight. After completion of the reaction, the reaction solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate system) to afford the target product dimethyl 4-bromophthalate (39.98 g, 66.1% yield) as a colorless oil. The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ (ppm) 3.90 (3H, s), 3.92 (3H, s), 7.63 (1H, d, J = 8.4 Hz), 7.68 (1H, dd, J = 2.0, 8.4 Hz), 7.84 (1H, d, J = 2.0 Hz).

References[1] Patent: US2002/19531, 2002, A1
Dimethyl 4-bromophthalate Preparation Products And Raw materials
Raw materials4-Bromo phthalic anhydrus-->Chlorosulfonic acid-->Methanol
Preparation Products3,3',4,4'-Biphenyltetracarboxylic acid
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