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Methyl 5-broMothiophene-3-carboxylate

CAS No.
88770-19-8
Chemical Name:
Methyl 5-broMothiophene-3-carboxylate
Synonyms
EA458;Methyl 2-bromothiophene-4-carboxylate;Methyl 5-broMothiophene-3-carboxylate;Methyl 5-bromo-3-thiophenecarboxylate;Methyl 5-bromothiophene-3-carboxylate 98%;5-Bromothiophene-3-carboxylic acid methyl ester;3-Thiophenecarboxylic acid, 5-bromo-, methyl ester
CBNumber:
CB72652875
Molecular Formula:
C6H5BrO2S
Molecular Weight:
221.07
MDL Number:
MFCD13386488
MOL File:
88770-19-8.mol
Last updated:2026-05-28 05:24:15

Methyl 5-broMothiophene-3-carboxylate Properties

Melting point 43-44 °C
Boiling point 244.6±20.0 °C(Predicted)
Density 1.662±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
Appearance Off-white to light brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
HS Code  2934999090

Methyl 5-broMothiophene-3-carboxylate price More Price(47)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth NDA77019 Methyl 5-bromo-3-thiophenecarboxylate 88770-19-8 10g $472 2026-06-04 Buy
Activate Scientific AS42428 Methyl 5-bromothiophene-3-carboxylate 97% 88770-19-8 1g $31 2026-06-04 Buy
Activate Scientific AS42428 Methyl 5-bromothiophene-3-carboxylate 97% 88770-19-8 5g $107 2026-06-04 Buy
Apolloscientific OR17258 Methyl 5-bromothiophene-3-carboxylate 99% 88770-19-8 1g $24 2026-06-04 Buy
Activate Scientific AS42428 Methyl 5-bromothiophene-3-carboxylate 97% 88770-19-8 25g $465 2026-06-04 Buy
Product number Packaging Price Buy
NDA77019 10g $472 Buy
AS42428 1g $31 Buy
AS42428 5g $107 Buy
OR17258 1g $24 Buy
AS42428 25g $465 Buy

Methyl 5-broMothiophene-3-carboxylate Chemical Properties, Uses, Production

Synthesis

Methanol

67-56-1

5-bromothiophene-3-carboxylic acid

100523-84-0

Methyl 5-broMothiophene-3-carboxylate

88770-19-8

1. Add a solution of bromine (2 mL, 39.06 mmol) in glacial acetic acid (64 mL) slowly dropwise to a stirred solution of 5-bromothiophene-3-carboxylic acid (5 g, 39.06 mmol) in glacial acetic acid (37 mL) at 0 °C. Stirring was done for 20 minutes at room temperature. The reaction mixture was poured into ice water with vigorous stirring. The white solid precipitate was collected by filtration, washed with water and recrystallized from hot water to give pure 5-bromothiophene-3-carboxylic acid bromide (Int-2) as a white solid (3.68 g, 46%).1H NMR (200 MHz, DMSO-d6): δ 7.55 (s, 1H), 8.17 (s, 1H). 2. Int-2 (3.4 g, 16.42 mmol) was dissolved in methanol (40 mL), H2SO4 (321 mg, 3.28 mmol) was added, and stirred at reflux for 12 hours. Volatiles were removed by distillation under reduced pressure and the residue was extracted with DCM (75 mL). The organic phase was washed sequentially with water (40 mL), saturated aqueous NaHCO3 (40 mL), brine (40 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to give pure methyl 5-bromothiophene-3-carboxylate (Int-3) as a colorless viscous oil (3.3 g, 91%).1H NMR (200 MHz, DMSO-d6): δ 7.98 (s, 1H), 7.44 (s, 1H), 3.87 (s, 3H). 3. Int-3 (0.5 g, 2.26 mmol) was dissolved in dioxane (25 mL), and Int-4 (0.51 g, 2.26 mmol), Pd(OAc)2 (105 mg, 0.45 mmol), xanthic acid (265 mg, 0.497 mmol) and Cs2CO3 (1.18 g, 3.62 mmol) were added. After vacuum degassing, the reaction was stirred at reflux for 20 h under N2 protection. The reaction mixture was concentrated under reduced pressure and purified by column chromatography with the product eluting with EtOAc. The mixture was further purified by preparative HPLC (140 mg) to give pure Int-5 as a yellow solid (80 mg, 10%). Mass spectrum (m/z): 366.0 [M++1]. 1H NMR (200 MHz, DMSO-d6): δ 9.50 (d, J=7 Hz, 1H), 8.51 (d, J=7 Hz, 1H), 8.56 (d, J=5.2 Hz, 1H), 7.74 (brs, 1H), 7.66 (d, J=11.8 Hz, 1H). 7.35 (d, J=7.4 Hz, 1H), 7.11 (s, 1H), 7.02 (d, J=5.6 Hz, 1H), 6.87 (t, J=6.8 Hz, 1H), 3.86 (s, 3H), 2.73 (s, 3H). 4. Int-5 (0.7 g, 1.91 mmol) was dissolved in THF:MeOH:H2O (2:1:2, 50 mL), LiOH (0.24 g, 5.74 mmol) was added, and heated and stirred at 50 °C for 16 hours. Volatiles were removed by distillation under reduced pressure and the reaction mixture was acidified to pH 5-6 with 2N HCl. The precipitated solid was filtered and dried under vacuum to give pure Int-6 (0.51 g, 76%). Mass spectrum (m/z): 352.0 [M++1]. 1H NMR (200 MHz, DMSO-d6): δ 12.45 (brs, 1H), 10.87 (s, 1H), 9.70 (brs, 1H), 8.60 (d, J=4.68 Hz, 1H), 7.67-7.59 (m, 2H), 7.45 (t, J=8.4 Hz, 1H), 7.13 (d, J=5.2 Hz, 1H), 7.04 (s, 2H), 2.65 (s, 3H).

References

[1] Patent: US2010/29638, 2010, A1. Location in patent: Page/Page column 110
[2] Tetrahedron Letters, 2013, vol. 54, # 11, p. 1460 - 1462
[3] Journal of Materials Chemistry C, 2018, vol. 6, # 14, p. 3731 - 3742
[4] Patent: WO2005/9941, 2005, A1. Location in patent: Page 43-44
[5] Patent: WO2011/33255, 2011, A1. Location in patent: Page/Page column 72

67-56-1
100523-84-0
88770-19-8
Synthesis of Methyl 5-broMothiophene-3-carboxylate from Methanol and 5-bromothiophene-3-carboxylic acid

Methyl 5-broMothiophene-3-carboxylate Preparation Products And Raw materials

Global Suppliers ( 81)
Supplier Tel Email Country ProdList Advantage
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View Latest Price from Methyl 5-broMothiophene-3-carboxylate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Methyl 5-broMothiophene-3-carboxylate pictures 2020-01-08 Methyl 5-broMothiophene-3-carboxylate
88770-19-8
$1.00 1g 99.0% 100kg Career Henan Chemical Co
Methyl 5-broMothiophene-3-carboxylate Methyl 2-bromothiophene-4-carboxylate 5-Bromothiophene-3-carboxylic acid methyl ester Methyl 5-bromo-3-thiophenecarboxylate Methyl 5-bromothiophene-3-carboxylate 98% 3-Thiophenecarboxylic acid, 5-bromo-, methyl ester EA458 88770-19-8