Sodium Hydroxide → HCID 67019688, compound
Reaction equation
C[O:2][C:3](=[O:21])[C:4]1[C:5](=[CH:10][C:11]([NH:14][CH2:15][C:16]2[O:17][CH:18]=[CH:19][CH:20]=2)=[CH:12][CH:13]=1)[C:6]([O:8]C)=[O:7].[OH-].[Na+]>C(O)C>[O:17]1[CH:18]=[CH:19][CH:20]=[C:16]1[CH2:15][NH:14][C:11]1[CH:10]=[C:5]([C:6]([OH:8])=[O:7])[C:4](=[CH:13][CH:12]=1)[C:3]([OH:21])=[O:2]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-[(furan-2-ylmethyl)-amino]-phthalic acid dimethyl ester (1.11 g, 3.84 mmol) and 3N sodium hydroxide (50 mL) in ethanol (100 mL) was refluxed for one hour. The reaction mixture was cooled to room temperature, and the solvent was removed under vacuum. The residue was dissolved in water (100 mL), washed with CH2Cl2 (2×100 mL) and acidified (HCl). The resulting mixture was extracted with ethyl acetate (2×100 mL), and the organic phase was washed with water (2×100 mL), and dried (MgSO4) and evaporated. The resulting solid was stirred in ether for 2 hours. The solid was filtered to give the 0.44 g of 4-[(furan-2-ylmethyl)-amino]-phthalic acid, in 44% yield; 1H NMR (DMSO-d6) δ 4.33 (d, J=5.1 Hz, 2H), 6.31 (d, J=3.0 Hz, 1H), 6.39 (dd, J=3.0 Hz, 1.8 Hz, 1H), 6.65-6.71 (m, 2H), 7.00 (t, J=5.7 Hz, 1H), 7.57-7.60 (m, 2H), 12.51 (br, 2H).
Workup
- temperaturewas refluxed for one hour
- customthe solvent was removed under vacuum
- dissolutionThe residue was dissolved in water (100 mL)
- washwashed with CH2Cl2 (2×100 mL)
- extractionThe resulting mixture was extracted with ethyl acetate (2×100 mL)
- washthe organic phase was washed with water (2×100 mL)
- dry with materialdried (MgSO4)
- customevaporated
- filtrationThe solid was filtered
Sources & evidence
- ORD record
- ord-f32cf060239a41329bf4aa5f9b25877d
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09447070B2
Reaction notes
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