HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-[(Thiochroman-8-YL)oxy]butyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 4-[(thiochroman-8-YL)oxy]butyrate | HCID 20093602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[(Thiochroman-8-YL)oxy]butyric acid | HCID 20093619 | — |
Reaction Steps
Under argon and with stirring, 2.25 g (8.02 mmol) of the compound obtained in Step A are dissolved in 30 cm3 of methanol. 4.5 cm3 of a 10% potassium hydroxide solution are added dropwise. After 2 hours at room temperature, the methanol is evaporated off. The residue is acidified very slowly with a 2N hydrochloric acid solution. The resulting precipitate is extracted with CH2Cl2 and dried over MgSO4. 1.94 g of a white solid are recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05332741 |
| Source dataset | uspto-grants-1994_07 |
| ORD ID | ord-0bc8b76f10a744dcbbb25f0fa075645a |
| Source note | uspto-grants-1994_07 |