HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732004Generated: October 28, 2026
Sodium Hydroxide → 3-Fluoro-5-(methoxycarbonyl)benzoic acid
https://huagongshe.com/reaction/732004
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethyl 5-fluoroisophthalate | HCID 4047226 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Fluoro-5-(methoxycarbonyl)benzoic acid | HCID 24728920 | 83% |
Reaction Steps
A suspension of 5-fluoro-isophthalic acid dimethyl ester (1.7 g, 8.0 mmol) in methanol (41 ml) was treated with 1.0 N sodium hydroxide (7.2 ml, 7.2 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 1.0 N HCl to pH 2. Ethyl acetate was used to extract the precipitate, which was then washed with brine and dried over anhydrous sodium sulphate. After removal of solvent in vacuo, a total of 1.3 g (83%) of 5-fluoro-isophthalic acid monomethyl ester was isolated as a white solid. 1H NMR (DMSO), δ (ppm): 8.31 (t, 1H), 7.96 (m, 2H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585881B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-19b3f5fd1e7c48a484c8e349f1fe1a1a |
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| Source note | uspto-grants-2009_09 |
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