HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Cyclopentyloxy-4-(methylthio)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-cyclopentyloxy-4-(methylthio)benzoate | HCID 21187944 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Cyclopentyloxy-4-(methylthio)benzoic acid | HCID 21187829 | — |
Reaction Steps
A suspension of methyl 3-cyclopentyloxy-4-(methylthio)benzoate (0.8 g; that is prepared as described in Reference Example 54) in methanol (10 mL) and water (5 mL) is treated with potassium carbonate (0.48 g) and the mixture is heated at reflux for 7 hours. The mixture is concentrated, and the resulting residue is partitioned between diethyl ether (20 mL) and water (20 mL). The aqueous layer is separated, acidified to pH 1 by treatment with dilute hydrochloric acid (2N), and extracted with dichloromethane (2×25 mL). The combined organic extracts are dried and concentrated, to give 3-cyclopentyloxy-4-(methylthio)benzoic acid (0.7 g) in the form of a white solid m.p. 150°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05698711 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-f7b2e195f7af427e9c6d149f84ad08e3 |
| Source note | uspto-grants-1997_12 |