HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791343Generated: October 26, 2026
Sodium Hydroxide → 3-Methoxy-5-(methoxycarbonyl)benzoic acid
https://huagongshe.com/reaction/1791343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethyl-5-methoxyisophthalate | HCID 4167302 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Methoxy-5-(methoxycarbonyl)benzoic acid | HCID 11020136 | 75.1% |
Reaction Steps
A suspension of dimethyl-5-methoxy-isophthalate (6.4 g, 28.5 mmol) in methanol (143 mL) was treated with 1 N sodium hydroxide (25.6 mL, 25.6 mmol). The reaction was left stirring overnight at room temperature. After the solution was concentrated, the residue was dissolved in water and transferred to a separatory funnel. The aqueous layer was washed with dichloromethane (3 times) and then acidified with 1 N HCl to pH 2. Ethyl acetate was used to extract the precipitate, which was then washed with brine and dried over anhydrous sodium sulfate. After removal of solvent in vacuo, 4.5 g (75%) of 5-methoxyisophthalic acid monomethyl ester was isolated as a white solid. 1H NMR (DMSO), δ(ppm): 8.17 (m, 1H), 7.60 (m, 2H), 3.80 (s, 3H), 3.76 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07074809B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-7993330f56544394abc27c1cca50f87f |
|---|
| Source note | uspto-grants-2006_07 |
|---|