HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → 2-(p-Benzoylphenoxy)ethylcarbamic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [4-(2-Aminoethoxy)phenyl]-phenylmethanone | HCID 3393464 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(p-Benzoylphenoxy)ethylcarbamic acid ethyl ester | HCID 53643529 | 61% |
Reaction Steps
5.5 g of 2-(p-benzoylphenoxy)ethylamine and 13 g of chloroformic acid ethyl ester are dissolved in 200 ml of acetone. 19.3 g of potassium carbonate are added to the solution and the mixture is heated under reflux with stirring for 30 hours. The mixture is then filtered and the crystals are washed with acetone. The filtrate is evaporated in vacuo. The residue is dissolved in ethyl acetate. The organic phase is washed with water, dried over sodium sulfate and evaporated in vacuo. The residue is dissolved in ether and crystallized by the addition of cyclohexane to yield 3.8 g (61%) of 2-(p-benzoylphenoxy)ethylcarbamic acid ethyl ester, m.p.--84°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04215139 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-e719c0ec2efb42e6bbace35dd5bcc22b |
| Source note | uspto-grants-1980_07 |