ChemicalBook--->CAS DataBase List--->2655-84-7

2655-84-7

2655-84-7 Structure

2655-84-7 Structure
IdentificationMore
[Name]

3-BROMOPHENETOLE
[CAS]

2655-84-7
[Synonyms]

1-BROMO-3-ETHOXYBENZENE
3-BROMOPHENETOLE
3-BROMOPHENYL ETHYL ETHER
3-ETHOXYBROMOBENZENE
AKOS 314
M-BROMOPHENETOLE
[EINECS(EC#)]

220-186-9
[Molecular Formula]

C8H9BrO
[MDL Number]

MFCD00274287
[Molecular Weight]

201.06
[MOL File]

2655-84-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

206 °C (lit.)
[density ]

1.481 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.548(lit.)
[Fp ]

182 °F
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow to Light orange
[Specific Gravity]

1.481
[InChI]

1S/C8H9BrO/c1-2-10-8-5-3-4-7(9)6-8/h3-6H,2H2,1H3
[InChIKey]

LQBMPJSTUHWGDE-UHFFFAOYSA-N
[SMILES]

CCOc1cccc(Br)c1
[CAS DataBase Reference]

2655-84-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2909309090
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMOPHENETOLE(2655-84-7)MS
3-BROMOPHENETOLE(2655-84-7)1HNMR
3-BROMOPHENETOLE(2655-84-7)IR1
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-Bromophenetole, 98%(2655-84-7)
[Sigma Aldrich]

2655-84-7(sigmaaldrich)
[TCI AMERICA]

3-Bromophenetole,>98.0%(GC)(2655-84-7)
Hazard InformationBack Directory
[Synthesis]

3-Bromophenol

591-20-8

Iodoethane

75-03-6

3-BROMOPHENETOLE

2655-84-7

General procedure for the synthesis of 3-ethoxybromobenzene: Sodium hydride (18.4 g, 60% oil dispersion, 460 mmol) was suspended in 1000 mL of DMF and the mixture was cooled to 0 °C. 3-Bromophenol (72 g, 419 mmol) was placed in a dropping funnel and heated using a hot air gun to melt it and then added dropwise to the cooled sodium hydride suspension. After the dropwise addition, the reaction mixture was continued to be stirred at 0 °C for 30 min. Subsequently, iodoethane (40 mL, 78 g, 503 mmol) was slowly added dropwise and the mixture was stirred for 12 hours, during which time it was allowed to warm naturally to room temperature. Upon completion of the reaction, water (1000 mL) was carefully added to quench the reaction, followed by extraction with ethyl acetate (4 x 500 mL). The organic layers were combined, washed with water (8 x 200 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The residue was distilled under reduced pressure and the fractions with boiling points above 120 °C were collected to give 70 g of the target product 3-ethoxybromobenzene in 84% yield. The density of the product was 1.47 g/mL.

[References]

[1] Patent: US5914329, 1999, A
[2] Patent: EP944611, 2004, B1. Location in patent: Page 6-7
[3] Patent: US2018/290997, 2018, A1. Location in patent: Paragraph 0209
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