HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577549Generated: October 30, 2026
Sodium Hydroxide → 3-Ethoxy-6-hydroxy-2-methylbenzoic acid
https://huagongshe.com/reaction/577549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | Methyl 6-bromo-3-ethoxy-2-methylbenzoate | HCID 86723776 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Ethoxy-6-hydroxy-2-methylbenzoic acid | HCID 86723777 | 79% |
Reaction Steps
A solution of methyl 6-bromo-3-ethoxy-2-methylbenzoate (114c, 0.298 g, 1.09 mmol) in DMSO (4 mL) was treated with 10M NaOH (1.0 mL, 10 mmol) and heated at 95° C. After 1 hour, the ester was hydrolyzed. The reaction mixture was cooled to room temperature and sodium bicarbonate (0.850 g, 10.1 mmol) and water (3 mL) were added. The suspension was sonicated until homogeneous. A solution of copper(II) sulfate (0.0348 g, 0.218 mmol) and trans-N,N′-dimethylcyclohexane-1,2-diamine (0.071 mL, 0.44 mmol) in water (2.0 mL) was added. The reaction mixture was heated at 95° C. for 1 hour. The reaction mixture was cooled to room temperature, poured into ethyl acetate, and washed with 1N HCl and brine. The organic layer was dried over Na2SO4 and concentrated under vacuum to give 3-ethoxy-6-hydroxy-2-methylbenzoic acid (114d, 0.168 g, 79% yield) as a salmon colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040515B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-02955aef4c42479d9c7cf881469b90a7 |
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| Source note | uspto-grants-2015_05 |
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