HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 5-(Hydroxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Formyl ketene | HCID 14931171 | — |
| Product | 5-(Hydroxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 11137577 | — |
Reaction Steps
Although the reaction mechanism is unknown, a process may be considered that at an intermediate step of the reaction, carbon dioxide, acetone and formyl ketene as intermediates are formed from formyl Meldrum's acid, and the formyl ketene reacts with the carbonyl compound to give the objective 1,3-dioxin-4-one derivative. In such a process, since the intermediate formyl ketene is extremely reactive, it is considered that resin formation is promoted in the case of high concentration reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04612379 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-657da6b17bb14ba6b4b1383f972fcad3 |
| Source note | uspto-grants-1986_09 |