HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 21411013, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Acetylethanolamine | HCID 8880 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1'-(Chloromethylene)bis(4-fluorobenzene) | HCID 2723773 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21411013 | HCID 21411013 | — |
Reaction Steps
A mixture of 25.4 g (0.1 mole) of bis(p-fluorophenyl)methyl chloride, 10.3 g (0.1 mole) of N-(2-hydroxyethyl)acetamide (prepared according to F. J. McQuillin et al., J. Chem. Soc. 1955, 2966), 14 g of potassium carbonate and 100 ml of benzene is refluxed for 5 hours. After cooling, the reaction mixture is poured into water. The aqueous layer is extracted with dichloromethane and the combined organic layers are dried over potassium carbonate and concentrated by evaporation of solvent. The residue is crystallised from toluene. N-{2-[Bis(p-fluorophenyl)methoxy]ethyl}acetamide, m.p. 112°-113.5° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049825 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-960ee825475f47fca5a303ae0e21606d |
| Source note | uspto-grants-1977_09 |