HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963108Generated: October 31, 2026
Potassium Hydroxide → HCID 13670762, compound
https://huagongshe.com/reaction/963108
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13670761 | HCID 13670761 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13670762 | HCID 13670762 | 72.8% |
Reaction Steps
Diethyl 2-(5-amino-4-(2-chlorobenzoyl)thiophen-2-ylmethyl)malonate (20 g) and a 4M potassium hydroxide aqueous solution (30 ml) were added to ethanol (120 ml), and the mixture was refluxed under heating for 2 hours. The solvent was evaporated, and the residue was dissolved in water. 1.2M Hydrochloric acid was added to adjust the solution to pH 3. The mixture was extracted with ethyl acetate to give a product and the product was washed with brine, and dried over magnesium sulfate. The solvent was evaporated. Dimethylformamide (30 ml) and toluene (70 ml) were added to the residue, and the mixture was heated at 80° C. for 1 hour. The mixture was washed with water, dried over magnesium sulfate and concentrated to give 11.0 g of 3-(5-amino-4-(2-chlorobenzoyl)thiophen-2-yl)propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760032 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-dda8c155d1e849e49345540008f7efe7 |
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| Source note | uspto-grants-1998_06 |
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