HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(1-Methylpropylsulphenyl)-4-trifluoromethylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(1-Methylpropylsulphenyl)-4-trifluoromethylbenzonitrile | HCID 54339387 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(1-Methylpropylsulphenyl)-4-trifluoromethylbenzoic acid | HCID 53811343 | — |
Reaction Steps
2-(1-Methylpropylsulphenyl)-4-trifluoromethylbenzonitrile (8.6 g), 10M sodium hydroxide (120 ml) and ethanol were combined and heated at reflux for 24 hours. The cooled mixture was poured into water and acidified to pH 1 with concentrated hydrochloric acid. The mixture was extracted with ethyl acetate. The organic phase was washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness yielding 2-(1-methylpropylsulphenyl)-4-trifluoromethylbenzoic acid (8.1 g) as a white solid, m.p. 99.8°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747424 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-b331539e5be44690b4bd024ea87d9468 |
| Source note | uspto-grants-1998_05 |