HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → (3,5-Dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3,5-Dichloro-4-hydroxy-phenyl)-carbamic Acid Tert-butyl Ester | HCID 22048528 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (3,5-Dichloro-4-ethoxy-phenyl)-carbamic acid tert-butyl ester | HCID 54404293 | — |
Reaction Steps
To a solution of (3,5-dichloro-4-hydroxy-phenyl)-carbamic acid tert-butyl ester (1.0 g) and potassium carbonate (1.0 g) in acetone (18 mL) is added ethyl iodide (0.36 mL) and the mixture is stirred for approximately 15 hours at room temperature. The solution is then filtered, concentrated under reduced pressure, and partitioned between ethyl acetate and water. The separated aqueous layer is further extracted twice with ethyl acetate, and the pooled organic extracts are washed successively with 10% aqueous sodium hydroxide, with water, and then dried over anhydrous sodium sulfate. Evaporation of the solvent under reduced pressure gave the desired product as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271236B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-6b3d63334cc84cdc80ced75494634ee7 |
| Source note | uspto-grants-2001_08 |