HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21268854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14663246 | HCID 14663246 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21268854 | HCID 21268854 | — |
Reaction Steps
A mixture of 2,4-dichloro-3-hydroxy-9-oxo-9H-xanthene (7.5 g), potassium carbonate (7.5 g), ethyl bromoacetate (9.0 g) and DMF (100 ml) was stirred at 55°-65° C. for 3 hours. After cooling the mixture, sodium hydroxide (20 g) and water (250 ml) were added and the resulting mixture was stirred at 90°-100° C. for 1 hour. After cooling, the mixture was rendered acidic with hydrochloric acid and the solid crystal was recovered by filtration, washed with water and dried. Recrystallization from ethanol gave 4.0 g of 2,4-dichloro-9-oxo-9H-xanthene-3-yloxyacetic acid. m.p. 225°-228° C. This compound gave a mass spectrum having a molecular ion peak at m/e 338.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661607 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-44b9db511e604f1ab71f6b7c333a6768 |
| Source note | uspto-grants-1987_04 |