HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2,2-diethoxyethyl Benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chloro-1,1-diethoxyethane | HCID 12128 | — |
| Reactant | Potassium Benzoate | HCID 23661960 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,2-diethoxyethyl Benzoate | HCID 11817258 | 84.8% |
Reaction Steps
Chloroacetaldehyde diethyl acetal (2.00 g), potassium benzoate (1.91 g), potassium iodide (0.41 g) and DMF (20 mL) were placed in a three-neck flask, followed by refluxing. Twenty hours later, the reaction mixture was cooled to room temperature, and water (30 mL) and ethyl acetate (80 mL) were added thereto, followed by stirring. After filtration, the organic layer was separated, was subjected to vacuum concentration and then to Kugelrohr distillation at 110-120° C. and at 1 mmHg and thereby yielded the target compound (2.41 g) in a yield of 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728152B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-b38bb05c9a654ded9acc8930760c2a49 |
| Source note | uspto-grants-2010_06 |