ChemicalBook--->CAS DataBase List--->46112-46-3

46112-46-3

46112-46-3 Structure

46112-46-3 Structure
IdentificationBack Directory
[Name]

4-(2-hydroxyethyl)benzoic acid
[CAS]

46112-46-3
[Synonyms]

4-(2-Hydroxyethyl)
4-(2-Hydroxyethyl)benzoic acid
Benzoic acid, 4-(2-hydroxyethyl)-
4-(2-Hydroxyethyl)benzoic acid 95%
[Molecular Formula]

C9H10O3
[MDL Number]

MFCD02114379
[MOL File]

46112-46-3.mol
[Molecular Weight]

166.17
Chemical PropertiesBack Directory
[Melting point ]

127-128 °C
[Boiling point ]

345.8±25.0 °C(Predicted)
[density ]

1.256±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.26±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P305+P351+P338
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(2-hydroxyethyl)benzoic acid(46112-46-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 4-(2-hydroxyethyl)benzoate

46190-45-8

4-(2-hydroxyethyl)benzoic acid

46112-46-3

General procedure for the synthesis of 4-(2-hydroxyethyl)benzoic acid from methyl 4-(2-hydroxyethyl)benzoate: sodium hydroxide (58 mg, 1.43 mmol) was added to a mixed solution of methanol (3 mL) and water (1 mL) of methyl 4-(2-hydroxyethyl)benzoate (174 mg, 0.96 mmol) at room temperature. The reaction mixture was stirred at room temperature for 48 hours. Upon completion of the reaction, water (5 mL) was added to dilute and extracted with ether (3 x 20 mL) to remove unreacted feedstock and by-products. The aqueous phase was acidified with a 1:1 hydrochloric acid solution to pH=1 and a white solid was precipitated. The solid was collected by filtration to afford 4-(2-hydroxyethyl)benzoic acid (158 mg, 100% yield), and the product could be used in the next reaction without further purification. The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 7.97 (d, J = 8.4 Hz, 2H), 7.27 (d, J = 8.4 Hz, 2H), 3.83 (t, J = 6.3 Hz, 2H), 2.88 (t, J = 6.3 Hz, 2H).

[References]

[1] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 11, p. 2988 - 2998
[2] Journal of the American Chemical Society, 2006, vol. 128, # 50, p. 16020 - 16021
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