HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761923Generated: November 1, 2026
Methyl 5-chloro-3-(1,3-dioxolan-2-yl)-2-hydroxybenzoate → Methyl 3-formyl-2-hydroxybenzoate
https://huagongshe.com/reaction/1761923
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 5-chloro-3-(1,3-dioxolan-2-yl)-2-hydroxybenzoate | HCID 19840310 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 3-formyl-2-hydroxybenzoate | HCID 345559 | 85.3% |
Reaction Steps
86 g of methyl 5-chloro-3-(1,3-dioxolan-2-yl)-2-hydroxybenzoate are dissolved in a mixture of 700 ml of methanol and 50 ml of tetrahydrofuran, and 70 ml of triethylamine and 7 g of 10% palladium-carbon are added to the solution. The mixture is subjected to catalytic hydrogenation under atmospheric pressure. The reaction mixture is filtered and the filtrate is evaporated to remove solvent. 10% hydrochloric acid is added to the residue and the mixture is concentrated. Water is added to the residue and the aqueous mixture is extracted with ethyl acetate. The extract is dried and evaporated to remove solvent. The resultant crystals are collected, washed with cold ethanol and dried to give 51.1 g of methyl 3-formyl-2-hydroxybenzoate as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04829067 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-9a691dd01d224518852de3522242e240 |
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| Source note | uspto-grants-1989_05 |
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