HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(Carboxy)-1-(4-methoxybenzylthio)cyclopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(Carbomethoxy)-1-(4-methoxybenzylthio)cyclopentane | HCID 15814381 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Carboxy)-1-(4-methoxybenzylthio)cyclopentane | HCID 15814382 | 72% |
Reaction Steps
Dissolve 1-(carbomethoxy)-1-(4-methoxylbenzylthio)cyclopentane (3.3 mmol) in 95% ethanol (18 mL), water (9 mL), and tetrahydrofuran (10 mL). Treat with potassium hydroxide (0.91 g, 16 mmol). Stir at room temperature for 2 hours and evaporate the solvent in vacuo. Partition between water (50 mL) and ethyl ether (30 mL). Acidify the aqueous phase with cold concentrated hydrochloric acid and extract with methylene chloride (50 mL). Dry (MgSO4) and evaporate the solvent in vacuo to give 1-(carboxy)-1-(4-methoxybenzylthio)cyclopentane as a pale yellow oil (483 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420271 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-279301e8fab645e2b646f9e68253eda6 |
| Source note | uspto-grants-1995_05 |