Hydrochloric Acid → 4-Ethoxy-3-methylbenzoic acid

HRID 713085Notes

Reaction equation

HRID 713085 reaction equation
[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][C:7]([C:8]([O:10]CC)=[O:9])=[CH:6][C:5]=1[CH3:15])[CH3:2].[OH-].[Na+].Cl>O.CO>[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][C:7]([C:8]([OH:10])=[O:9])=[CH:6][C:5]=1[CH3:15])[CH3:2]

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 68291767Ethyl 4-ethoxy-3-methylbenzoate

Product 1

HCID 301475274-Ethoxy-3-methylbenzoic acidYield 64%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

The crude ethyl 4-ethoxy-3-methyl-benzoate was suspended in a solution of NaOH (10.5 g, 263 mmol) in water (50 mL) and methanol (25 mL). The reaction mixture was refluxed for 1 h. The reaction mixture was cooled to 0° C., acidified with 12 M HCl (24.7 mL, 296 mmol) and the resulting solid filtered. The solid was slurried with acetonitrile and filtered to provide 4-ethoxy-3-methyl-benzoic acid (760 mg, 4.22 mmol, 64%) as a light pink solid. ESI-MS m/z calc. 180.07864. found 181.3 (M+1)+; Retention time: 1.31 minutes (3 min run). 1H NMR (400 MHz, DMSO-d6) δ 12.50 (s, 1H), 7.77 (dd, J=8.5, 2.2 Hz, 1H), 7.73 (d, J=1.5 Hz, 1H), 7.00 (d, J=8.6 Hz, 1H), 4.11 (q, J=7.0 Hz, 2H), 2.17 (s, 3H), 1.36 (t, J=7.0 Hz, 3H).

Workup

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. filtrationthe resulting solid filtered
  3. filtrationfiltered

Sources & evidence

ORD record
ord-00814c338d0342638c8d618ccd524660
Source dataset
uspto-grants-2015_11
Patent number
US09181273B2

Reaction notes

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