HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21268855, 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 15617012 | HCID 15617012 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21268855 | HCID 21268855 | 79.6% |
Reaction Steps
A mixture of 3-hydroxy-2-methyl-9-oxo-9H-xanthene (1.8 g), potassium carbonate (2.2 g), ethyl bromoacetate (2.7 g) and DMF (40 ml) was stirred at 60°-70° C. for 2 hours. After cooling the mixture, sodium hydroxide (3.2 g) and water (40 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 1.8 g of 2-methyl-9-oxo-9H-xanthene-3-yloxyacetic acid. m.p. 236°-238° C. This compound showed a mass spectrum having a molecular ion peak at m/e 284.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816479 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-04a6dc7f66d349ea855c1024ad3cd0e1 |
| Source note | uspto-grants-1989_03 |