HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → Trimethylolpropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2,2-dimethylolbutanal | HCID 11051693 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | Trimethylolpropane | HCID 6510 | — |
Reaction Steps
In the Cannizzaro process, butyraldehyde is reacted with formaldehyde in the presence of a stoichiometric amount of base. This initially forms 2,2-dimethylolbutanal which then reacts with a further molecule of formaldehyde in a cross-Cannizzaro reaction to form formic acid and trimethylolpropane. The disadvantage of this method is that one molar equivalent of formate is formed as coproduct. This has to be worked up and increases the consumption of formaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112707B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-6aa0d5f8ece7413e94ed676c01255609 |
| Source note | uspto-grants-2006_09 |