ChemicalBook--->CAS DataBase List--->1128-76-3

1128-76-3

1128-76-3 Structure

1128-76-3 Structure
IdentificationMore
[Name]

ETHYL 3-CHLOROBENZOATE
[CAS]

1128-76-3
[Synonyms]

3-CHLOROBENZOIC ACID ETHYL ESTER
ETHYL 3-CHLOROBENZOATE
RARECHEM AL BI 0056
Benzoic acid, m-chloro-, ethyl ester
Ethyl m-chlorobenzoate
Ethyl 3-chlorobenzoate, 98+%
[EINECS(EC#)]

214-441-3
[Molecular Formula]

C9H9ClO2
[MDL Number]

MFCD00013634
[Molecular Weight]

184.62
[MOL File]

1128-76-3.mol
Chemical PropertiesBack Directory
[Boiling point ]

118-120°C 13mm
[density ]

1,186 g/cm3
[refractive index ]

1.5220
[Fp ]

118-120°C/13mm
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow
[BRN ]

2045877
[CAS DataBase Reference]

1128-76-3(CAS DataBase Reference)
[EPA Substance Registry System]

Benzoic acid, 3-chloro-, ethyl ester (1128-76-3)
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[TSCA ]

TSCA listed
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 3-CHLOROBENZOATE(1128-76-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Ethyl 3-chlorobenzoate, 98+%(1128-76-3)
[TCI AMERICA]

Ethyl 3-Chlorobenzoate,>94.0%(GC)(1128-76-3)
Hazard InformationBack Directory
[Synthesis]

CHLOROETHANE

75-00-3

3-Chlorobenzoic acid

535-80-8

ETHYL 3-CHLOROBENZOATE

1128-76-3

Under stirring conditions, 3-chlorobenzoic acid (1.00 mmol), chloroethane (1.20 mmol), and IL-1 (0.30 mmol) were sequentially added to a two-necked flask containing 6 mL of 50% aqueous ethanol solution. Subsequently, the temperature of the reaction system was raised to 70 °C and maintained at this temperature in a water bath. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reactor was cooled to room temperature. The reaction mixture was diluted with 10 mL of water and extracted with ethyl acetate (3 x 5 mL). The organic phases were combined, dried over anhydrous Na2SO4 and filtered, and the filtrate was concentrated in a rotary evaporator to give ethyl m-chlorobenzoate. The catalyst was dried under vacuum at 80 °C for 6 h after removing the solvent and could be recycled for the next round of reaction. All esterification products need to be further purified by column chromatography.

[References]

[1] Catalysis Letters, 2017, vol. 147, # 11, p. 2764 - 2771
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