(4-BROMO-2-THIENYL)METHANOL
(4-BROMO-2-THIENYL)METHANOL Basic information
- Product Name:
- (4-BROMO-2-THIENYL)METHANOL
- Synonyms:
-
- 4-BROMO-2-(HYDROXYMETHYL)THIOPHENE
- (4-BROMO-2-THIENYL)METHANOL
- RARECHEM AL BD 0179
- (4-BroMothien-2-yl)Methanol
- 2-Thiophenemethanol, 4-bromo-
- 4-Bromothiophene-2-methanol
- 4-Bromo-2-thiophenemethanol
- CAS:
- 79757-77-0
- MF:
- C5H5BrOS
- MW:
- 193.06
- Product Categories:
-
- Building Blocks
- Thiophene
- Mol File:
- 79757-77-0.mol
(4-BROMO-2-THIENYL)METHANOL Chemical Properties
- Melting point:
- 30 °C
- Boiling point:
- 271.5±25.0 °C(Predicted)
- Density
- 1.772±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- solubility
- soluble in Methanol
- form
- powder to lump
- pka
- 13.50±0.10(Predicted)
- color
- White to Orange to Green
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 20/21/22-36/37/38-41-22
- Safety Statements
- 26-36/37/39-39
- HS Code
- 2934999090
(4-BROMO-2-THIENYL)METHANOL Usage And Synthesis
Synthesis
18791-75-8
79757-77-0
Step I: Sodium borohydride (5.20 g, 0.137 mol) was added batchwise to a solution of 4-bromo-2-thiophenecarboxaldehyde (25.0 g, 0.131 mol) in anhydrous tetrahydrofuran (400 mL). The reaction mixture was stirred at room temperature for 1.5 hours. Upon completion of the reaction, saturated ammonium chloride solution (100 mL) was slowly added to quench the reaction. Subsequently, the reaction mixture was extracted with ethyl acetate and the organic phases were combined and washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford (4-bromo-2-thienyl)methanol (25.02 g, 99% yield), and the product could be used for subsequent reactions without further purification. NMR hydrogen spectrum (400 MHz, CDCl3): δ = 1.93 (broad single peak, 1H), 4.79 (single peak, 2H), 6.93 (single peak, 1H), 7.18 (double peak, J = 1.5 Hz, 1H).
References
[1] Journal of the American Chemical Society, 2007, vol. 129, # 24, p. 7523 - 7530
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 4, p. 1788 - 1792
[3] Synthesis, 1983, # 1, p. 73 - 75
[4] Patent: WO2013/110643, 2013, A1. Location in patent: Paragraph 00212; 00213
[5] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 4, p. 1992 - 2010
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(4-BROMO-2-THIENYL)METHANOL(79757-77-0)Related Product Information
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- SPECS AI-942/25034100
- RARECHEM AL BI 0455
- SPECS AP-836/41220404