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dimethyl 2,5-dibromoterephthalate

CAS No.
18014-00-1
Chemical Name:
dimethyl 2,5-dibromoterephthalate
Synonyms
Einecs 241-919-9;dimethyl 2,5-dibromoterephthalate;2,5-Dibromo-terephthalic acid dimethyl ester;2,5-dibromobenzene-1,4-dicarboxylic acid dimethyl ester;1,4-Benzenedicarboxylicacid, 2,5-dibromo-, 1,4-dimethyl ester
CBNumber:
CB7921634
Molecular Formula:
C10H8Br2O4
Molecular Weight:
351.98
MDL Number:
MFCD00204592
MOL File:
18014-00-1.mol
MSDS File:
SDS
Last updated:2026-05-28 04:17:13

dimethyl 2,5-dibromoterephthalate Properties

Melting point 148.6 °C
Boiling point 362.0±37.0 °C(Predicted)
Density 1.781±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Appearance White to off-white Solid
InChI InChI=1S/C10H8Br2O4/c1-15-9(13)5-3-8(12)6(4-7(5)11)10(14)16-2/h3-4H,1-2H3
InChIKey QXAFZEQRMJNPLY-UHFFFAOYSA-N
SMILES C1(C(OC)=O)=CC(Br)=C(C(OC)=O)C=C1Br

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338

dimethyl 2,5-dibromoterephthalate price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
AstaTech 60472 DIMETHYL 2,5-DIBROMOTEREPHTHALATE 97% 18014-00-1 5G $29 2026-04-30 Buy
AstaTech 60472 DIMETHYL 2,5-DIBROMOTEREPHTHALATE 97% 18014-00-1 25G $129 2026-04-30 Buy
AstaTech 60472 DIMETHYL 2,5-DIBROMOTEREPHTHALATE 97% 18014-00-1 100G $483 2026-04-30 Buy
Matrix Scientific 097805 Dimethyl 2,5-dibromoterephthalate 18014-00-1 5.00g $88 2026-05-18 Buy
Matrix Scientific 097805 Dimethyl 2,5-dibromoterephthalate 18014-00-1 25.00g $398 2026-05-18 Buy
Product number Packaging Price Buy
60472 5G $29 Buy
60472 25G $129 Buy
60472 100G $483 Buy
097805 5.00g $88 Buy
097805 25.00g $398 Buy

dimethyl 2,5-dibromoterephthalate Chemical Properties, Uses, Production

Chemical Properties

white powder

Synthesis

Methanol

67-56-1

2,5-Dibromoterephthalic acid

13731-82-3

dimethyl 2,5-dibromoterephthalate

18014-00-1

1. Iodine (78 mg, 0.33 mmol) was added to p-xylene (6.13 mL, 50.0 mmol) at 0 °C, followed by the addition of bromine (5.20 mL, 101 mmol) dropwise over 10 min. After removal of the ice bath, the reaction mixture was stirred for 16 h at room temperature under light protected conditions. The reaction was quenched with 20% KOH aqueous solution and stirred for 15 min until the solution was colorless. The solid precipitate was collected by filtration and washed twice with 100 mL of water. Recrystallization by ethanol gave a white solid product (9.19 g, 70% yield).1H NMR (CDCl3) data: δ 7.40 (s, 2H), 2.34 (s, 6H). 2. 1,4-Dibromo-2,5-dimethylbenzene (5.93 g, 22.5 mmol) and KMnO4 (15.72 g, 99.5 mmol) were dissolved in 80 mL of t-BuOH:H2O (1:1) mixed solvent, and refluxed for 18 h after adding diatomaceous earth (14 g). The reaction mixture was cooled to room temperature, filtered through diatomaceous earth and the filter cake was washed with hot water (100 mL) and EtOAc (50 mL). The filtrate was acidified to pH=1 with concentrated hydrochloric acid and the white suspension formed was extracted three times with EtOAc (100 mL). The organic phases were combined, dried over MgSO4 and concentrated under reduced pressure to give a white solid product (3.06 g, 42% yield) without further purification.1H NMR (DMSO-d6) data: δ 8.01 (s, 2H). 3. 2,5-Dibromoterephthalic acid (2.04 g, 6.30 mmol) was dissolved in 35 mL of methanol and refluxed for 30 min, then thionyl chloride (9.00 mL, 124 mmol) was slowly added and refluxing was continued for 12 hours. The reaction mixture was cooled to room temperature, 50 mL of water was carefully added and extracted three times with Et2O (75 mL). The organic phases were combined, washed three times with saturated NaHCO3 solution (50 mL), dried over MgSO4 and concentrated under reduced pressure. The solid was recrystallized by methanol to give a white crystalline product (1.65 g, 74% yield) with a melting point of 134-136 °C (literature value 134-137 °C).1H NMR (CDCl3) data: δ 8.06 (s, 2H), 3.96 (s, 6H), in agreement with known spectra.

References

[1] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 5, p. 1781 - 1783
[2] Journal of the American Chemical Society, 1994, vol. 116, # 26, p. 11723 - 11736
[3] Tetrahedron, 2015, vol. 71, # 2, p. 283 - 292
[4] Journal of Organic Chemistry, 1959, vol. 24, p. 26
[5] Bulletin de la Societe Chimique de France, 1958, p. 1418,1420

dimethyl 2,5-dibromoterephthalate Preparation Products And Raw materials

Raw materials

Preparation Products

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dimethyl 2,5-dibromoterephthalate Spectrum

dimethyl 2,5-dibromoterephthalate 2,5-Dibromo-terephthalic acid dimethyl ester Einecs 241-919-9 1,4-Benzenedicarboxylicacid, 2,5-dibromo-, 1,4-dimethyl ester 2,5-dibromobenzene-1,4-dicarboxylic acid dimethyl ester 18014-00-1 C10H8Br2O4 Derivatives of phthalic acid