HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → Ethyl 2-fluorocyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Ethyl 2-chloro-2-fluorocyclopropanecarboxylate | HCID 9793930 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-fluorocyclopropanecarboxylate | HCID 10313150 | 88.9% |
Reaction Steps
An internal glass tube was introduced into an autoclave and 0.5 g of ethyl 2-chloro-2-fluoro-1-cyclopropanecarboxylate (cis:trans=1.4:1), 0.5 ml of Raney nickel and 5 ml of ethanol were fed thereinto. Then 0.54 g of 1,2-diaminoethane was further added and the mixture was stirred at room temperature under an elevated hydrogen gas atmosphere (50 kgf/cm2) for 24 hours. After the completion of the reaction, the catalyst was filtered off. Then the reaction mixture was analyzed by gas chromatography. As a result, it was found out that the reaction conversion rate was 100%, the yield was 88.9% and the cis:trans ratio was 1.4:1. The analytical data of the title compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780669 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-39c16876bab74c65b9c98ee6a7a7ec9e |
| Source note | uspto-grants-1998_07 |