ChemicalBook--->CAS DataBase List--->35287-42-4

35287-42-4

35287-42-4 Structure

35287-42-4 Structure
IdentificationBack Directory
[Name]

4-bromo-2-(bromomethyl)-1-nitrobenzene
[CAS]

35287-42-4
[Synonyms]

5-bromo-2-nitrobenzyl bromide
4-bromo-2-(bromomethyl)-1-nitrobenzene
Benzene, 4-bromo-2-(bromomethyl)-1-nitro-
[EINECS(EC#)]

233-305-4
[Molecular Formula]

C7H5Br2NO2
[MDL Number]

MFCD11848689
[MOL File]

35287-42-4.mol
[Molecular Weight]

294.93
Chemical PropertiesBack Directory
[Boiling point ]

330.2±27.0 °C(Predicted)
[density ]

2.006±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

crystalline solid
[color ]

Light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P305+P351+P338
[HS Code ]

2904990090
Spectrum DetailBack Directory
[Spectrum Detail]

4-bromo-2-(bromomethyl)-1-nitrobenzene(35287-42-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

(5-bromo-2-nitrophenyl)methanol

1241894-37-0

4-bromo-2-(bromomethyl)-1-nitrobenzene

35287-42-4

To a stirred solution of (5-bromo-2-nitrophenyl)methanol (2.8 g, 12.06 mmol) in a solvent mixture of dichloromethane (DCM) and acetonitrile (MeCN) (1:1, 100 mL) was added sequentially at 0 °C carbon tetrabromide (CBr4) (5.2 g, 15.68 mmol) and triphenylphosphine (PPh3) (4.1 g. 15.68 mmol). The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was purified by fast column chromatography on silica gel (petroleum ether (PE)/ethyl acetate (EA) = 50:1 to 10:1 gradient elution) to afford the target product 4-bromo-2-(bromomethyl)-1-nitrobenzene (1.1 g, 31% yield).

[References]

[1] Patent: WO2018/68017, 2018, A1. Location in patent: Page/Page column 154; 155; 156; 157
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