HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581062Generated: November 1, 2026
2,3-Dihydroxybenzoic Acid → 2,3-Dihydro-1,4-benzodioxin-5-carboxylic acid
https://huagongshe.com/reaction/581062
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydroxybenzoic Acid | HCID 19 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3-Dihydro-1,4-benzodioxin-5-carboxylic acid | HCID 78184 | — |
Reaction Steps
A mixture of 10.8 g (70 mmol) of 2,3-dihydroxybenzoic acid, 38.6 g (280 mmol) of dry potassium carbonate and 24 ml (278 mmol) of 1,2-dibromoethane in 40 ml of N,N-dimethylformamide is heated at 65° C. for 24 hours under an inert atmosphere. After cooling, the reaction mixture is diluted with water and then extracted with ether. The aqueous phase is then acidified with a 3N hydrochloric acid solution and subsequently extracted with dichloromethane. After removal of the solvent by evaporation in vacuo, the residue obtained is recrystallised from toluene to yield the title acid in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919814 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-21253bf35f474d2d90338f4eb2cf3cb0 |
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| Source note | uspto-grants-1999_07 |
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