ChemicalBook--->CAS DataBase List--->22802-37-5

22802-37-5

22802-37-5 Structure

22802-37-5 Structure
IdentificationBack Directory
[Name]

4-BROMO-2,3-DIMETHYLPHENOL
[CAS]

22802-37-5
[Synonyms]

4-BROMO-2,3-DIMETHYLPHENOL
2,3-Dimethyl-4-bromophenol
Phenol, 4-bromo-2,3-dimethyl-
[Molecular Formula]

C8H9BrO
[MDL Number]

MFCD07778969
[MOL File]

22802-37-5.mol
[Molecular Weight]

201.06
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light brown to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMO-2,3-DIMETHYLPHENOL(22802-37-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,3-dimethylphenol

526-75-0

4-BROMO-2,3-DIMETHYLPHENOL

22802-37-5

GENERAL METHODS: 2,3-Dimethylphenol (1 mmol) was dissolved in acetonitrile (5 mL), OXBTEATB (0.233 g, 0.5 mmol) was added, and the reaction was stirred at room temperature until the appropriate time (Table 1). The reaction process was monitored by thin layer chromatography (TLC) (eluent ratio: hexane/ethyl acetate = 5/1). Upon completion of the reaction, OXBTEATB was removed by filtration, and the filtrate was transferred to a partition funnel and extracted sequentially with water (15 mL) and dichloromethane (20 mL). The organic layers were combined and dried with anhydrous Na2SO4, followed by concentration on a rotary evaporator to remove solvent. The crude product was purified by silica gel column chromatography, the eluent being a solvent mixture of hexane and ethyl acetate. To regenerate the reagents, the resulting white solid was treated with liquid bromine. The structures of all products were analyzed by melting point determination or 1H NMR spectroscopy and confirmed by comparison with data reported in the literature [29a-29e].

[References]

[1] Letters in Organic Chemistry, 2018, vol. 15, # 8, p. 682 - 687
[2] Bulletin of the Chemical Society of Japan, 1987, vol. 60, # 11, p. 4187 - 4189
[3] Tetrahedron, 2007, vol. 63, # 34, p. 8242 - 8249
[4] Synthetic Communications, 2010, vol. 40, # 6, p. 868 - 876
[5] Tetrahedron, 2003, vol. 59, # 18, p. 3201 - 3217
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