ChemicalBook--->CAS DataBase List--->22532-60-1

22532-60-1

22532-60-1 Structure

22532-60-1 Structure
IdentificationBack Directory
[Name]

Benzaldehyde, 2-broMo-4-hydroxy
[CAS]

22532-60-1
[Synonyms]

2-BroMo-4-Hydroxy benzaldehyde
Benzaldehyde, 2-broMo-4-hydroxy
[EINECS(EC#)]

801-622-2
[Molecular Formula]

C7H5BrO2
[MDL Number]

MFCD16999767
[MOL File]

22532-60-1.mol
[Molecular Weight]

201.02
Chemical PropertiesBack Directory
[Boiling point ]

292.4±20.0 °C(Predicted)
[density ]

1.737±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

6.81±0.18(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C7H5BrO2/c8-7-3-6(10)2-1-5(7)4-9/h1-4,10H
[InChIKey]

OCBOCCOUCDGNKX-UHFFFAOYSA-N
[SMILES]

C(=O)C1=CC=C(O)C=C1Br
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

Benzaldehyde, 2-broMo-4-hydroxy(22532-60-1)1HNMR
Benzaldehyde, 2-broMo-4-hydroxy(22532-60-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

3-Bromophenol

591-20-8

Benzaldehyde, 2-broMo-4-hydroxy

22532-60-1

The general procedure for the synthesis of 2-bromo-4-hydroxybenzaldehyde from ethanol and m-bromophenol was as follows: 30% aqueous sodium hydroxide solution (160 mL) was mixed with 3-bromophenol (10.04 g, 58 mmol) and heated to 70-75 °C. Subsequently, ethanol (5 mL) was added all at once and chloroform (28 mL, 0.35 mol) was added slowly and dropwise. After maintaining the reaction at 75 °C for 1 hour, the reaction mixture was continued to be stirred at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and acidified with 10N hydrochloric acid. Most of the by-products were removed by steam distillation. The residue was cooled and the precipitate was separated by filtration. The crude product was purified by silica gel column chromatography using hexane/ethyl acetate (2:1, v/v) as eluent to give 1.75 g of 2-bromo-4-hydroxybenzaldehyde in 15% yield.

[References]

[1] Patent: WO2011/37731, 2011, A1. Location in patent: Page/Page column 111-112
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