HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → Formate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Formate | HCID 283 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Product | Formate | HCID 283 | — |
| Product | Trimethylolpropane | HCID 6510 | — |
Reaction Steps
In the process of the invention, n-butyraldehyde is firstly reacted with formaldehyde in the presence of a base. This reaction can be carried out in one or more stages. In the single-stage variant, the starting materials are reacted directly to form trimethylolpropane and a formate salt. In a two-stage variant, n-butyraldehyde and formaldehyde are firstly reacted in the presence of catalytic amounts of base to form 2,2-dimethylolbutanal, purification or separation steps are carried out if desired and only then is the 2,2-dimethylolbutanal reacted with further formaldehyde in the presence of stoichiometric amounts of base to form trimethylolpropane and formate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448455B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-aa8dfbb3fb5d424bb2bb06948722cbea |
| Source note | uspto-grants-2002_09 |