Hydrochloric Acid → 3-Methoxybenzoic Acid
Reaction equation
[OH-].[Na+].C[O:4][C:5](=[O:16])[C:6]1[CH:11]=[CH:10][C:9](CN)=[C:8]([O:14][CH3:15])[CH:7]=1.Cl.CCN(CC)CC.C1C2C(COC(ON3C(=O)CCC3=O)=O)C3C(=CC=CC=3)C=2C=CC=1>CO.CC#N>[CH3:15][O:14][C:8]1[CH:7]=[C:6]([CH:11]=[CH:10][CH:9]=1)[C:5]([OH:16])=[O:4]Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 40 °C
Procedure
A 1 N solution of NaOH (6.15 mL; 6.14 mmol) was added dropwise to a solution of 4-(aminomethyl)-3-methoxybenzoic acid methyl ester C (1.2 g; 6.14 mmol) in MeOH (25 mL) heated at 40° C. After stirring 8 h at 45° C. the solution was stirred over night at room temperature. A 1 N solution of NaOH (0.6 mL; 0.6 mmol) was added and the mixture heated at 40° C. for 4 h. The solution was concentrated, acidified with 1 N HCl (8 mL; 8 mmol), extracted with EtOAc (2×10 mL) then the aqueous layer was concentrated to 15 mL. This solution (pH 4.5) was cooled at 0° C. and Et3N (936 μL; 6.75 mmol) was added (pH 11). A solution of N-(9-fluorenylmethoxycarbonyloxy)succinimide (3.04 g; 9 mmol) in MeCN (30 mL) was added dropwise (final pH 9) and a white solid precipitated. After stirring 1 h at room temperature the solid was filtered, suspended in 1N HCl (15 mL) and the suspension was stirred for 30 min. The solid was filtered to provide 4-[[[9H-fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methoxybenzoic acid E as a white solid (275 mg; 0.7 mmol).
Workup
- stirringwas stirred over night at room temperature
- temperaturethe mixture heated at 40° C. for 4 h
- concentrationThe solution was concentrated
- extractionextracted with EtOAc (2×10 mL)
- concentrationthe aqueous layer was concentrated to 15 mL
- temperatureThis solution (pH 4.5) was cooled at 0° C.
- customprecipitated
- stirringAfter stirring 1 h at room temperature the solid
- filtrationwas filtered
- stirringthe suspension was stirred for 30 min
- filtrationThe solid was filtered
Sources & evidence
- ORD record
- ord-c58d29ebc8b546ceafeca6cf223a2c7a
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07850947B2
Reaction notes
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