Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19922602 | HCID 19922602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15289642 | HCID 15289642 | 88.2% |
Reaction Steps
5 g of methyl-2-[3-chloro-4-(2-oxocyclopentane-1-yl methyl)phenyl]propionate were incorporated with 80 ml of an aqueous methanol containing 2.9 g of potassium hydroxide and then refluxed under heat for two hours. After the completion of the reaction, the reaction mixture obtained was treated to concentrate the solvent at a reduced pressure, incorporated with 50 ml of water, washed with 50 ml of ethyl acetate, after which the aqueous layer obtained was adjusted to a pH of 2 with conc. hydrochloric acid, thereafter extracted with 60 ml of ether, washed with water, dried and then freed of the solvent to obtain a residue. The thus obtained residue was distilled at a reduced pressure thereby to obtain 4.2 g (yield 88%) of oily 2-[3-chloro-4-(2-oxocyclopentane-1-yl methyl)phenyl]propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434292 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-05226784c23a41aa980331927c003f05 |
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| Source note | uspto-grants-1995_07 |
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