HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-Carboxy-2-(4-methoxybenzylthio)indan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(Carbomethoxy)-2-(4-methoxybenzylthio)indan | HCID 15280734 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Carboxy-2-(4-methoxybenzylthio)indan | HCID 15280735 | 43% |
Reaction Steps
Dissolve 2-(carbomethoxy)-2-(4-methoxybenzylthio)indane (2.20 g, 3.55 mmol) in 95% ethanol (25 mL), water (12 mL) and tetrahydrofuran (15 mL). Treat with potassium hydroxide (1.3 g, 23 mmol) and stir at room temperature for 1 hour. Filter and evaporate the solvent in vacuo. Partition between water (125 mL) and ether (75 mL). Separate the aqueous phase and acidify with cold concentrated hydrochloric acid. Extract with methylene chloride (75 mL), dry (Na2SO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography (2:1 hexane/ethyl acetate) to give 2-carboxy-2-(4-methoxybenzylthio)indane as a yellow solid (0.48 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05604221 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-3b4f47a0a38e488e9137f155664cfb09 |
| Source note | uspto-grants-1997_02 |