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(4-Bromo-3-fluorophenyl)methanol

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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 Structure
(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
pka13.70±0.10(Predicted)
color White to Almost white
Safety Information
HS Code 2906290090
MSDS Information
(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
4-Bromo-3-fluorobenzoic acid

153556-42-4

(4-BROMO-3-FLUOROPHENYL)METHANOL

222978-01-0

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
Raw materialsMethyl 4-bromo-3-fluorobenzoate 98-->4-Bromo-3-fluorobenzoic acid-->4-Bromo-3-fluorobenzaldehyde-->Borane THF-->Tetrahydrofuran
Preparation Products4-(Bromomethyl)-2-fluorobenzonitrile
Tag:(4-Bromo-3-fluorophenyl)methanol(222978-01-0) Related Product Information
Methyl 4-bromo-3-fluorobenzoate 98 4-Bromo-2,3,5,6-tetrafluorobenzoic acid 4-Bromo-3-fluorobenzoic acid 4-Bromo-2,3,5,6-tetrafluorobenzylalcohol (4-Bromo-3-fluorophenyl)methanol 4-bromo-2,5-difluorobenzoic acid 4-Bromo-2,3-difluorobenzoic acid 4-Bromo-2-chloro-5-fluorobenzoic acid tert-Butyl 4-bromo-3-fluorobenzoate 4-Bromo-2,3,6-trifluorobenzyl alcohol 4-Bromo-3-fluorobenzoic acid ethyl ester 4-Bromo-5-fluoro-2-nitrobenzoic acid 2-Amino-4-bromo-5-fluorobenzoic acid ethyl 4-bromo-2,3,5,6-tetrafluorobenzimidate RARECHEM AL BP 1308 RARECHEM AL BI 1308 RARECHEM AL BF 1308 tert-Butyl 4-bromo-2,3,5,6-tetrafluorobenzoate