Basic information Safety Supplier Related

4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER

Basic information Safety Supplier Related

4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER Basic information

Product Name:
4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER
Synonyms:
  • 4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER
  • Benzoic acid, 4-chloro-3-hydroxy-, methyl ester
CAS:
166272-81-7
MF:
C8H7ClO3
MW:
186.59
Mol File:
166272-81-7.mol
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4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER Chemical Properties

Melting point:
100-101 °C
Boiling point:
288.3±20.0 °C(Predicted)
Density 
1.354±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
7.68±0.10(Predicted)
Appearance
Light brown to brown Solid
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Safety Information

HS Code 
2918290090
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4-CHLORO-3-HYDROXY-BENZOIC ACID METHYL ESTER Usage And Synthesis

Uses

4-Chloro-3-hydroxybenzoic Acid Methyl Ester id used in the synthesis of antidepressants.

Synthesis

67-56-1

34113-69-4

166272-81-7

The general procedure for the synthesis of methyl 3-hydroxy-4-chlorobenzoate from methanol and 4-chloro-3-hydroxybenzoic acid was as follows: thionyl chloride (6 g) was added slowly and dropwise to a methanol (100 mL) solution of 4-chloro-3-hydroxybenzoic acid (4.4 g, 25.50 mmol). The reaction mixture was stirred at 70 °C for 2 hours. Upon completion of the reaction, the reaction solution was concentrated under reduced pressure to remove the solvent. The concentrated residue was diluted by adding hexane (50 mL) to the concentrated residue. The precipitated solid product was collected by filtration and dried in an oven under reduced pressure to afford methyl 3-hydroxy-4-chlorobenzoate as a light yellow solid (4 g, 84% yield). The product was analyzed by LC/MS (electrospray ionization, m/z): [M+H]+ 187.0. 1H NMR (300 MHz, DMSO-d6) δ 10.69 (s, 1H, OH), 7.55 (d, J=2.10 Hz, 1H, ArH), 7.49 (d, J=8.40 Hz, 1H, ArH), 7.36-7.40 ( m, 1H, ArH), 3.83-3.85 (d, J=8.40Hz, 3H, OCH3).

References

[1] Chemical and Pharmaceutical Bulletin, 1994, vol. 42, # 11, p. 2365 - 2369
[2] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 13, p. 3141 - 3147
[4] Journal of Medicinal Chemistry, 2005, vol. 48, # 9, p. 3290 - 3312
[5] Patent: EP2048140, 2009, A1. Location in patent: Page/Page column 25

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