HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Ethyl alpha-iodo-3-chloro-4-cyclohexylphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethyl alpha-bromo-3-chloro-4-cyclohexylphenylacetate | HCID 21454151 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl alpha-iodo-3-chloro-4-cyclohexylphenylacetate | HCID 21454139 | — |
Reaction Steps
A mixture of 40.5 g. (0.1 moles) of ethyl α-bromo-3-chloro-4-cyclohexylphenylacetate and 150 g. of sodium iodide in 1 liter of anhydrous acetone is refluxed for 4 hours. The reaction mixture is then evaporated to dryness and extracted with ether. The ether is then washed with water, dried and evaporated to dryness to obtain ethyl α-iodo-3-chloro-4-cyclohexylphenylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04008269 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-fb8e13dbca504f08ad2b7e6d63363ee4 |
| Source note | uspto-grants-1977_02 |