Hydrochloric Acid → (5-Methyl-2-nitrophenyl)acetic acid
Reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:19]([O-:21])=[O:20])=[C:6]([CH:8](C(OCC)=O)[C:9]([O:11]CC)=[O:10])[CH:7]=1.Cl>C(O)(=O)C.O.CC#N>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:19]([O-:21])=[O:20])=[C:6]([CH2:8][C:9]([OH:11])=[O:10])[CH:7]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
Diethyl 2-(5-methyl-2-nitro-phenyl)propanedioate (9.50 g, 32.2 mmol) was suspended in glacial acetic acid (40 mL) and warmed until it had dissolved. Hydrochloric acid (40 mL of 6 M solution, 240.0 mmol) was added dropwise and the solution heated at reflux for 24 h. After cooling to room temperature the reaction was diluted with water and extracted with ether. The ether was dried over Na2SO4, filtered, and concentrated in vacuo to afford a light orange solid. The solid was dissolved in minimal CH3CN and added dropwise to stirring 0.05 N HCl (300 mL) resulting in a beige precipitate. The suspension was cooled in an ice bath, filtered, and washed with water to obtain 2-(5-methyl-2-nitro-phenyl)acetic acid as a beige crystalline solid (5.30 g, 84% yield). LC/MS m/z 391.4 [M+H]+. 1H NMR (400.0 MHz, DMSO-d6) δ 12.51 (s, 1H), 8.01 (d, J=8.9 Hz, 1H), 7.36 (m, 2H), 3.95 (s, 2H), 2.40 (s, 3H).
Workup
- temperaturewarmed until it
- dissolutionhad dissolved
- temperaturethe solution heated
- temperatureat reflux for 24 h
- extractionextracted with ether
- dry with materialThe ether was dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto afford a light orange solid
- additionadded dropwise
- customresulting in a beige precipitate
- temperatureThe suspension was cooled in an ice bath
- filtrationfiltered
- washwashed with water
Sources & evidence
- ORD record
- ord-68ffbcea0c9042d0bf7c923c4c6f958b
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367660B2
Reaction notes
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