Basic information Safety Supplier Related

Methyl 3,4-dichlorophenylacetate

Basic information Safety Supplier Related

Methyl 3,4-dichlorophenylacetate Basic information

Product Name:
Methyl 3,4-dichlorophenylacetate
Synonyms:
  • METHYL 3,4-DICHLOROPHENYLACETATE
  • 3,4-DICHLOROPHENYLACETIC ACID METHYL ESTER
  • Dichlorophenyl acetic acid methyl ester
  • Methyl 3,4-dichlorophenylacetate, 97+%
  • 2-(3,4-dichlorophenyl)acetic acid methyl ester
  • Methyl2-(3,4-dichlorophenyl)acetate
  • Methyl 3,4-dichlorophenylacetate,99%
  • Methyl3,4-Dichlorophenylacetate>
CAS:
6725-44-6
MF:
C9H8Cl2O2
MW:
219.06
Product Categories:
  • Aromatic Esters
Mol File:
6725-44-6.mol
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Methyl 3,4-dichlorophenylacetate Chemical Properties

Melting point:
25-27
Boiling point:
314.25°C (rough estimate)
Density 
1.54-1.542
refractive index 
1.54-1.542
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid After Melting
color 
Clear colorless to light yellow
CAS DataBase Reference
6725-44-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-37-26
Hazard Note 
Irritant
HS Code 
29163990

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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Methyl 3,4-dichlorophenylacetate Usage And Synthesis

Chemical Properties

clear colorless liquid

Synthesis

67-56-1

5807-30-7

6725-44-6

The general procedure for synthesizing methyl 3,4-dichlorophenylacetate from methanol and 3,4-dichlorophenylacetic acid was as follows: referring to Synthesis Example 1, methanol (59 mL, 3.0 equiv) was added to a solution of 1,2-dichloroethane (400 mL) containing 3,4-dichlorophenylacetic acid (100 g, 0.488 mol). The mixed solution was heated to 50 °C, followed by the slow dropwise addition of concentrated sulfuric acid (10 mL) over 15 min. After the dropwise addition was completed, the reaction temperature was maintained at 50°C and stirring was continued for 1.5 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and a partitioning operation was performed to separate and remove the sulfuric acid layer. The resulting organic layer was washed sequentially with water, saturated aqueous sodium bicarbonate solution and saturated brine, followed by drying with anhydrous magnesium sulfate. After drying, the desiccant was removed by filtration and the solvent was removed by distillation, resulting in the target product methyl 3,4-dichlorophenylacetate (105 g, yield: 98%) in the form of colorless oil. The structure of the product was confirmed by 1H-NMR (300 MHz, CDCl3) with chemical shifts δ: 3.59 (s, 2H), 3.71 (s, 3H), 7.12 (dd, J = 8.4 Hz, 1.8 Hz, 1H), 7.38-7.41 (m, 2H).

References

[1] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2843 - 2866
[2] Journal of Medicinal Chemistry, 2001, vol. 44, # 17, p. 2701 - 2706
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 9, p. 3618 - 3625
[4] Patent: US2003/225283, 2003, A1. Location in patent: Page 12-13
[5] Patent: EP2246343, 2010, A1. Location in patent: Page/Page column 10

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