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| | (4-Bromo-3-fluorophenyl)methanol Basic information |
| Product Name: | (4-Bromo-3-fluorophenyl)methanol | | Synonyms: | 4-Bromo-3-fluorobenzenemethanol;BenzeneMethanol, 4-broMo-3-fluoro-;4-Bromo-3-fluorobenzylalcohol,96%;(4-BROMO-3-FLUOROPHENYL)METHANOL ISO 9001:2015 REACH;3-Fluoro-4-Bromobenzyl alcohol;(4-Bromo-3-fluorophenyl)methanol | | CAS: | 222978-01-0 | | MF: | C7H6BrFO | | MW: | 205.02 | | EINECS: | | | Product Categories: | | | Mol File: | 222978-01-0.mol |  |
| | (4-Bromo-3-fluorophenyl)methanol Chemical Properties |
| Melting point | 44.0 to 48.0 °C | | Boiling point | 260℃ | | density | 1.658 | | Fp | 111℃ | | storage temp. | Sealed in dry,Room Temperature | | solubility | soluble in Methanol | | form | powder to crystal | | pka | 13.70±0.10(Predicted) | | color | White to Almost white |
| | (4-Bromo-3-fluorophenyl)methanol Usage And Synthesis |
| Uses | (4-Bromo-3-fluorophenyl)methanol is used to prepare triazolopyridyl compounds, which can be used as a prodrug of RIPK1 inhibitors. | | Synthesis | GENERAL METHODS: Borane-tetrahydrofuran complex (BH3-THF, 89 mL, 89.49 mmol) was slowly added dropwise to a stirred solution of 3-fluoro-4-bromobenzoic acid (9.8 g, 44.75 mmol) in tetrahydrofuran (THF, 200 mL) at 25 °C. The dropwise addition was controlled to be completed in 10 min, and the reaction was carried out under nitrogen protection. The reaction mixture was stirred continuously at room temperature for 2 days. Upon completion of the reaction, the reaction was carefully quenched with 2 M sodium carbonate solution (Na2CO3, 200 mL) and subsequently extracted with ether (Et2O, 2 x 500 mL). The organic phases were combined, washed with saturated brine (400 mL), dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to give a pale yellow oil. The crude product was purified by fast silica gel column chromatography, the eluent was a mixture of heptane and ethyl acetate (EtOAc) with a gradient elution ratio of 0 to 70% ethyl acetate. The purified fraction was collected and concentrated to dryness under reduced pressure to give 4-bromo-3-fluorobenzyl alcohol (8.65 g, 94% yield) as a white solid. | | References | [1] Journal of Medicinal Chemistry, 2014, vol. 57, # 21, p. 9096 - 9104 [2] Journal of Medicinal Chemistry, 2003, vol. 46, # 14, p. 2973 - 2984 [3] Synlett, 2014, vol. 25, # 1, p. 123 - 127 [4] European Journal of Medicinal Chemistry, 2018, vol. 150, p. 506 - 524 [5] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 10, p. 1257 - 1260 |
| | (4-Bromo-3-fluorophenyl)methanol Preparation Products And Raw materials |
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