HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893988Generated: October 30, 2026
Hydrochloric Acid → 5-[2-Hydroxy-3-(methylsulfanyl)propoxy]-4-oxo-4H-1-benzopyran-2-carboxylic acid
https://huagongshe.com/reaction/893988
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 5-(2-hydroxy-3-methylthiopropoxy)chromone-2-carboxylate | HCID 12888660 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-[2-Hydroxy-3-(methylsulfanyl)propoxy]-4-oxo-4H-1-benzopyran-2-carboxylic acid | HCID 3086067 | 89.8% |
Reaction Steps
To a solution of 3.4 g of ethyl 5-(2-hydroxy-3-methylthiopropoxy)chromone-2-carboxylate in 20 ml of acetone there is added 11 ml of N sodium hydroxide and the mixture is heated at 50° C. for 10 minutes. After evaporating the solvent under reduced pressure, 30 ml of water are added, the resulting mixture is extracted with diethyl ether, filtered on charcoal and the limpid solution thus obtained is acidified with hydrochloric acid. The product which precipitates is filtered, washed with water and dried. Thus, 2.8 g of 5-(2-hydroxy-3-methylthiopropoxy)chromone-2-carboxylic acid is obtained as dihydrate (CM 57202); m.p. 76°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282247 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-df7d36e322714315860f889fb0aac1f0 |
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| Source note | uspto-grants-1981_08 |
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