HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-Aminobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Aminobenzaldehyde | HCID 68255 | 96% |
Reaction Steps
Under nitrogen, 12.3 g (13.6 mmol) lithium cobalt (I) phthalocyanine x 4.5 THF and 322 mg (2 mmol) O-nitrobenzaldehyde are agitated in 65 ml methanol for 90 hours at 20° C. The green reaction mixture is mixed with 10 ml water; CO2 and air are passed in for 5 min., and the blue precipitate is centrifuged which is washed with ethanol. The centrifugate collected is concentrated, and the residue separated into ether and water. Concentration of the ether phase, dried with sodium sulfate, produces 230 mg (96%) O-amino benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04372893 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-45c9f7aa91b646298f95ca153d8b1484 |
| Source note | uspto-grants-1983_02 |