HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260719Generated: October 26, 2026
Sodium Hydroxide → 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid
https://huagongshe.com/reaction/260719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 5-Methyl-2,3-dihydrobenzo[B][1,4]dioxine-6-carbaldehyde | HCID 15767557 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carboxylic acid | HCID 10702959 | 61% |
Reaction Steps
In 5 ml of tetrahydrofuran was dissolved 0.8 g of 5-methyl-1,4-benzodioxan-6-carbaldehyde, then 27 ml of a 1% sodium hydroxide aqueous solution was added dropwise to the solution and further 0.5 g of a 10% palladium-carbon was added thereto, and the mixture was refluxed under heating for 1.5 days. The mixture was cooled to room temperature, 10 ml of a 10% sodium sulfite aqueous solution was added thereto and after stirring for 30 minutes, the mixture was filtered and the tetrahydrofuran was removed under reduced pressure. The residue was adjusted to pH 3 with a 5% hydrochloric acid and extracted with diethyl ether. The diethyl ether layer was washed successively with water and saturated saline solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to obtain 0.53 g of the titled 5-methyl-1,4-benzodioxan-6-carboxylic acid (yield: 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05530021 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-622b5c3acffe4cab80a7ba51011c7730 |
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| Source note | uspto-grants-1996_06 |
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