HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 4,5,6,7-Tetrahydro-1-benzofuran-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5,6,7-Tetrahydro-1-benzofuran-4-one | HCID 2733541 | 68% |
Reaction Steps
To a mixture of 1.12 g (10 mmoles) of 1,3-cyclohexanedione and 8 ml of water was added 1.38 g (10 mmoles) of potassium carbonate, and then 2 ml of 40% aqueous solution of chloroacetaldehyde was added thereto. The resulting mixture was stirred at a room temperature for 45 hours. The reaction mixture was maintained at a pH of from 7.75 to 9.50 throughout the reaction. After completing the reaction, the obtained reaction mixture was treated and analyzed in the same manner as in Example 1. It was proved from the results of the analysis that 4-oxo-4,5,6,7-tetrahydrobenzofuran was produced in a 68% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558143 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-3acf00d91bd24845bfb054d1ec170446 |
| Source note | uspto-grants-1985_12 |