Hydrochloric Acid → 3-(3-Chloropropoxy)-4-methoxybenzoic acid
Reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[O:16][CH3:17])[C:9]([O:11]C)=[O:10].[OH-].[Na+].Cl>CO>[Cl:1][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[O:16][CH3:17])[C:9]([OH:11])=[O:10]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
In a 300 mL volume glass flask equipped with a stirrer, a thermometer and a dropping funnel were placed 18.2 g (69.7 mmol) of methyl 3-(3-chloropropoxy)-4-methoxybenzoate, 69.7 mL of aqueous sodium hydroxide solution (2 mol/L), and 69.7 mL of methanol. The resulting mixture was heated to 40° C. for 4 hours in an argon gas atmosphere. After the reaction was complete, the reaction mixture was cooled to 10° C., and neutralized by 69.7 mL of hydrochloric acid (2 mol/L), to precipitate a crystalline product. The crystalline product was collected and dried under reduced pressure, to give 7.2 g (isolated yield: 95.8%, purity: 99% in terms of area percentage by high performance liquid chromatography) of 3-(3-chloropropoxy)-4-methoxybenzoic acid as a white crystalline product.
Workup
- customIn a 300 mL volume glass flask equipped with a stirrer
- temperaturethe reaction mixture was cooled to 10° C.
- customto precipitate a crystalline product
- customThe crystalline product was collected
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-e467454aefa74ed3a2f9ea871dac7df2
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367824B2
Reaction notes
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