ETHYL 3-CHLOROBENZOATE
ETHYL 3-CHLOROBENZOATE Basic information
- Product Name:
- ETHYL 3-CHLOROBENZOATE
- Synonyms:
-
- Benzoic acid, m-chloro-, ethyl ester
- Ethyl m-chlorobenzoate
- ETHYL 3-CHLOROBENZOATE
- 3-CHLOROBENZOIC ACID ETHYL ESTER
- NSC 67339
- RARECHEM AL BI 0056
- Ethyl 3-chlorobenzoate, 98+%
- Ethyl 3-Chlorobenzoate >
- CAS:
- 1128-76-3
- MF:
- C9H9ClO2
- MW:
- 184.62
- EINECS:
- 214-441-3
- Product Categories:
-
- Aromatic Esters
- Benzoic acid
- Acids & Esters
- Chlorine Compounds
- Mol File:
- 1128-76-3.mol
ETHYL 3-CHLOROBENZOATE Chemical Properties
- Boiling point:
- 118-120°C 13mm
- Density
- 1,186 g/cm3
- refractive index
- 1.5220
- Flash point:
- 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 Information
- Safety Statements
- 24/25
- HS Code
- 2916399090
MSDS
- Language:English Provider:ALFA
ETHYL 3-CHLOROBENZOATE Usage And Synthesis
Synthesis
75-00-3
535-80-8
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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