Ethyl 2-Chlorobenzoate
Ethyl 2-Chlorobenzoate Basic information
- Product Name:
- Ethyl 2-Chlorobenzoate
- Synonyms:
-
- ETHYL 2-CHLOROBENZOATE
- ETHYL O-CHLOROBENZOATE
- RARECHEM AL BI 0018
- O-CHLOROBENZOIC ACID ETHYL ESTER
- ETHYL 2-CHLOROBENZOATE 98%
- Ethyl 2-chlorobenzoate, 98+%
- 2-CHLOROBENZOIC ACID ETHYL ESTER
- ETHYL 2-CHLOROBENZOA
- CAS:
- 7335-25-3
- MF:
- C9H9ClO2
- MW:
- 184.62
- EINECS:
- 230-842-6
- Product Categories:
-
- Chlorine Compounds
- C8 to C9
- Carbonyl Compounds
- Esters
- Aromatic Esters
- Benzoic acid
- Acids & Esters
- Mol File:
- 7335-25-3.mol
Ethyl 2-Chlorobenzoate Chemical Properties
- Boiling point:
- 241-243 °C(lit.)
- Density
- 1.18 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.523(lit.)
- Flash point:
- >230 °F
- storage temp.
- Store at room temperature
- form
- clear liquid
- color
- Colorless to Almost colorless
- Specific Gravity
- 1.180
- BRN
- 2207359
- CAS DataBase Reference
- 7335-25-3(CAS DataBase Reference)
- EPA Substance Registry System
- Benzoic acid, 2-chloro-, ethyl ester (7335-25-3)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- HS Code
- 29163990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
Ethyl 2-Chlorobenzoate Usage And Synthesis
Chemical Properties
Clear colorless to pale yellow liquid
Synthesis
383-63-1
898768-95-1
7335-25-3
288310-94-1
GENERAL PROCEDURE: In a dry Schlenk tube, sodium hydride (6.0 mmol) was stirred with ethyl trifluoroacetate (6.0 mmol) in tetrahydrofuran (5 mL) for 10 minutes at room temperature under argon protection. Subsequently, a solution of enolizable ketone (5.0 mmol) in tetrahydrofuran (5 mL) was slowly added dropwise to the above mixture at 0°C and under argon atmosphere. The reaction solution was stirred at a set temperature for 2 to 6 hours before being cooled again to 0°C and the reaction was quenched with 6 mL of a 1 mol/L hydrochloric acid solution. After continued stirring for 15 minutes, the mixture was neutralized with saturated sodium bicarbonate solution. After conventional post-treatment steps, the residue was purified by silica gel column chromatography to give the target product trifluoromethyl alkyl ketone.
References
[1] Tetrahedron, 2014, vol. 70, # 31, p. 4668 - 4674
Ethyl 2-Chlorobenzoate Preparation Products And Raw materials
Raw materials
Preparation Products
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Ethyl 2-Chlorobenzoate(7335-25-3)Related Product Information
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