HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-[(2-Oxo-2-phenylethyl)thio]-5-(trifluoromethyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21542284 | HCID 21542284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[(2-Oxo-2-phenylethyl)thio]-5-(trifluoromethyl)benzoic acid | HCID 21544480 | — |
Reaction Steps
A mixture of 1.33 g. (6 m moles) of 3-mercapto-5-trifluoromethylbenzoic acid, 12 ml. of 1N sodium hydroxide solution and 930 mg. (6 m moles) of α-chloroacetophenone in 20 ml. of ethanol is allowed to stir at room temperature for 1 hour. The reaction mixture is diluted with water, extracted with ether and the resulting aqueous phase acidified with 12N hydrochloric acid. The light yellow oil which separates gradually crystallizes and is filtered, 1.8 g., m.p. 135°-150° C. A sample is sublimed at 165° C. and 0.05 mm pressure, m.p. 153°-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953595 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-e36e3b0729484a2ea375cfaa31e9e3ec |
| Source note | uspto-grants-1976_04 |