Basic information Safety Supplier Related

methyl 4-bromo-3-methylthiophene-2-carboxylate

Basic information Safety Supplier Related

methyl 4-bromo-3-methylthiophene-2-carboxylate Basic information

Product Name:
methyl 4-bromo-3-methylthiophene-2-carboxylate
Synonyms:
  • methyl 4-bromo-3-methylthiophene-2-carboxylate
  • 4-bromo-3-methyl-2-Thiophenecarboxylic acid methyl ester
  • 4-Bromo-3-methyl-thiophene-2-carboxylic acid methyl ester
  • 2-Thiophenecarboxylic acid, 4-bromo-3-methyl-, methyl ester
CAS:
265652-38-8
MF:
C7H7BrO2S
MW:
235.1
Mol File:
265652-38-8.mol
More
Less

methyl 4-bromo-3-methylthiophene-2-carboxylate Chemical Properties

Melting point:
61-61.5 °C
Boiling point:
263.3±35.0 °C(Predicted)
Density 
1.575±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Appearance
Off-white to gray Solid
More
Less

methyl 4-bromo-3-methylthiophene-2-carboxylate Usage And Synthesis

Synthesis

81452-54-2

265652-38-8

Step 2: Synthesis of methyl 4-bromo-3-methylthiophene-2-carboxylate: Methyl 3-methylthiophene-2-carboxylate (20 g, 103 mmol, 1.0 eq.) and sodium hydroxide (12.3 g, 307 mmol, 3 eq.) were dissolved in acetic acid (75 mL) and heated to 60 °C. Bromine (46.9 g, 294 mmol, 2.85 eq.) was added slowly dropwise with controlled titration rate to maintain the temperature of the reaction mixture below 85 °C. The reaction mixture was stirred continuously at 85 °C for 6 hours. Subsequently, the solution was cooled to 50 °C and zinc powder (15.4 g, 236 mmol, 2.3 eq.) was added in batches, ensuring that the temperature did not exceed 85 °C after each addition. After addition, the mixture was continued to be stirred at 85 °C for 1 h. The mixture was then thermally filtered through a preheated bed of small diatomaceous earth. Water (300 mL) was added to the filtrate and extracted with hexane (300 mL). The organic phase was washed with water and concentrated to dryness to give 27 g (89% yield) of an off-white oil, which gradually crystallized after standing at room temperature. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 7.43 (s, 1H), 3.87 (s, 3H), 2.56 (s, 3H).

References

[1] Patent: WO2012/56478, 2012, A1. Location in patent: Page/Page column 76
[2] Patent: US2018/170948, 2018, A1. Location in patent: Paragraph 0469
[3] Patent: WO2017/31213, 2017, A1. Location in patent: Paragraph 00385
[4] Patent: US2007/244094, 2007, A1. Location in patent: Page/Page column 40
[5] Justus Liebigs Annalen der Chemie, 1938, vol. 536, p. 135,142

methyl 4-bromo-3-methylthiophene-2-carboxylateSupplier

Chengdu Forest Science and Technology Development Co., Ltd.
Tel
18030648795
Email
sales@cdforestchem.com
Shanghai Taifu Pharmaceutical Technology Co. LTD
Tel
021-58111238 18930958102
Email
sales@taifupharm.com
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66028182 18626450290
Email
yftan@aikonchem.com
Cool Pharm, Ltd
Tel
021-60455363 18019463053
Email
sales@coolpharm.com
SuZhou ShiYa Biopharmaceuticals, Inc.
Tel
0512-0512-52358471 17715136450
Email
sales@shiyabiopharm.com
More
Less

methyl 4-bromo-3-methylthiophene-2-carboxylate(265652-38-8)Related Product Information