HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenol → HCID 2444863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one | HCID 1988398 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 2444863 | HCID 2444863 | 52.2% |
Reaction Steps
28.4 g (0.1 mol) of 2-bromoacetyl-5-bromothiophene are heated under reflux with 19.3 g (0.15 mol) of 4-chlorophenol and 27.6 g (0.2 mol) of potassium carbonate in 200 ml of ketone for 3 hours, while stirring. The mixture is then poured into water, and the ether-ketone is extracted with methylene chloride. The organic phase is washed with dilute sodium hydroxide solution and then with water, and is dried over magnesium sulphate. After the organic phase has been evaporated down, the residue is recrystallized from ethanol. 17.3 g (52% of theory) of 2-bromo-thien-5-yl 4-chlorophenoxymethyl ketone of melting point 128°-130° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596815 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-3ac0f2151258437cb69d9272fb3f75c4 |
| Source note | uspto-grants-1986_06 |