HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Tributylphosphine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 86743661 | HCID 86743661 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tributylphosphine | HCID 13831 | — |
| Product | HCID 86743660 | HCID 86743660 | — |
Reaction Steps
In 10.0 g of water was dissolved 10.0 g of tri-n-butylmethylphosphonium carbonate obtained as in Example 12 (1st step) and a solution of 4.2 g of maleic acid dissolved in 5.0 g of water was gradually added to the solution, whereby carbon dioxide simultaneously generated vigorously. For more completely removing carbon dioxide, degassing was performed for 2 hours at 40° C. and 20 mmHg and after confirming carbonate ions being less than 2 ppm, water was distilled off. The residue formed was recrystallized from methyl ethyl ketone to produce 1-1.2 g (94.1% of the theoretical yield, yield of 59.8% to tri-n-butylphosphine) of tri-n-butylmethylphosphonium monomaleate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892944 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-5ab61bab052f4c1da1c1530b5098c1ce |
| Source note | uspto-grants-1990_01 |