HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Trimethylolpropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2,2-dimethylolbutanal | HCID 11051693 | — |
| Product | Trimethylolpropane | HCID 6510 | — |
Reaction Steps
EP-A 860 419, too, proposes carrying out the preparation of 2,2-dimethylolbutanal from n-butyraldehyde and formaldehyde in a plurality of stages, with the actual reaction occurring in the first stage and the 2-ethylacrolein obtained as by-product being reacted with further formaldehyde in the second stage. The 2,2-dimethylolbutanal prepared in this way can then be hydrogenated to give trimethylolpropane. Once again, no formate is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448455B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-ba6d4dcd2b1044a7b3b416a567079934 |
| Source note | uspto-grants-2002_09 |