HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635223Generated: October 25, 2026
Hydrochloric Acid → 7-hydroxy-2-(hydroxymethyl)-chromen-4-one
https://huagongshe.com/reaction/635223
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | ethyl 7-hydroxy-4-oxo-4H-chromen-2-carboxylate | HCID 5376802 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-hydroxy-2-(hydroxymethyl)-chromen-4-one | HCID 10511929 | 66% |
Reaction Steps
To a suspension of 5 g (21 mmoles) of ethyl 7-hydroxy-4-oxo-chromen-2-carboxylate and 5 g (45 mmoles) of anhydrous calcium chloride in 100 mL of absolute ethanol, cooled at 0° C., were added 3 g of sodium borohydride in several portions and the mixture was stirred at room temperature for 16 hours. Further 1 g of sodium borohydride was added and stirred for an additional 2 hours. The reaction mixture was suspended in 200 mL of water and acidified slowly with HCl. The precipitate was filtered, washed with water and dried at vaccum to give 2.7 g de 7-hydroxy-2-(hydroxymethyl)-chromen-4-one as a solid, yield 66%, mp 250-252° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187793B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-6c5b322ea8f54b968525a0ef69da2925 |
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| Source note | uspto-grants-2001_02 |
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