methyl 4-bromo-3-methylthiophene-2-carboxylate
- Product Name
- methyl 4-bromo-3-methylthiophene-2-carboxylate
- CAS No.
- 265652-38-8
- Chemical 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
- CBNumber
- CB12995767
- Molecular Formula
- C7H7BrO2S
- Formula Weight
- 235.1
- MOL File
- 265652-38-8.mol
methyl 4-bromo-3-methylthiophene-2-carboxylate Property
- 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
N-Bromosuccinimide Price
- Product number
- BB20-2707
- Product name
- 4-Bromo-3-methyl-thiophene-2-carboxylicacidmethylester
- Purity
- 95%
- Packaging
- 5G
- Price
- $270
- Updated
- 2021/12/16
- Product number
- CM317737
- Product name
- Methyl4-bromo-3-methylthiophene-2-carboxylate
- Purity
- 95%
- Packaging
- 10g
- Price
- $401
- Updated
- 2021/12/16
- Product number
- CD41001430
- Product name
- Methyl4-bromo-3-methylthiophene-2-carboxylate
- Purity
- 95+%
- Packaging
- 10g
- Price
- $429
- Updated
- 2021/12/16
- Product number
- 265652388
- Product name
- Methyl4-bromo-3-methylthiophene-2-carboxylate
- Packaging
- 10g
- Price
- $437.58
- Updated
- 2021/12/16
- Product number
- CM317737
- Product name
- Methyl4-bromo-3-methylthiophene-2-carboxylate
- Purity
- 95%
- Packaging
- 25g
- Price
- $755
- Updated
- 2021/12/16
methyl 4-bromo-3-methylthiophene-2-carboxylate Chemical Properties,Usage,Production
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-carboxylate Preparation Products And Raw materials
Raw materials
Preparation Products
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