HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 20352251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | 1-Phenyl-3-azabicyclo[3.1.0]hexane | HCID 10130094 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20352251 | HCID 20352251 | — |
Reaction Steps
To a solution of 6.2 g. of p-fluorophenylacetic acid in 60 ml. of dry tetrahydrofuran is added 6.8 g. of N,N'-carbonyl diimidazole. The resultant mixture is allowed to stand 1 hour, at which time the evolution of carbon dioxide has ceased. To this solution is added 6.4 g. of 1-phenyl-3-azabicyclo[3.1.0]hexane and the reaction solution is allowed to stand 1/2 hour and then warmed on a steam bath for 1/2 hour. After removal of the solvent, the residue is poured into ice-water and the mixture is extracted with chloroform. The extracts are dried and evaporated to give the product as an amber oil; IR 6.04μ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088652 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-b0f8035f8a984cc3b144e0e7f9054ad0 |
| Source note | uspto-grants-1978_05 |