HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78697Generated: October 25, 2026
Boron trifluoride etherate → 2-Hydroxy-4,5-dimethoxybenzoic acid
https://huagongshe.com/reaction/78697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2,4,5-Trimethoxybenzoic acid | HCID 10276 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Hydroxy-4,5-dimethoxybenzoic acid | HCID 11564650 | 91% |
Reaction Steps
In 10 g of ethyl acetate were suspended 2.0 g of 2,4,5-trimethoxybenzoic acid (1a) and 1.45 g of NaBr in a stream of argon, to which 4.0 g of BF3.Et2O was then added dropwise at 25° C., followed by heat stirring at 40° C. for 3 hours. The reaction mixture was cooled with ice, to which 10 mL of water was then added dropwise at 10° C., followed by dropwise adding 7.5 g of a 25% (w/w) sodium hydroxide aqueous solution. Thereto was further added 10 mL of water before stirring, followed by filtering off insoluble inorganic matter. To the separated aqueous layer was dropwise added 3.94 g of 35% hydrochloric acid, followed by stirring for 10 minutes. The precipitated crystal was collected by filtration and washed with water. The resultant crystal was then dried under reduced pressure at 60° C. to provide 1.7 g of 2-hydroxy-4,5-dimethoxybenzoic acid (2a) at a yield of 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841461B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a5126c13cb174211811fcc74d1968deb |
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| Source note | uspto-grants-2014_09 |
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