HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivalaldehyde → Retinal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | 2,2-Dimethyl-3,4-pentadienal | HCID 77678 | — |
| Reactant | 2,2-Dimethylpent-4-enal | HCID 79636 | — |
| Reactant | 2,2-Dimethylvaleraldehyde | HCID 84292 | — |
| Reactant | Butanal, 2,2-dimethyl- | HCID 137426 | — |
| Reactant | HCID 15174357 | HCID 15174357 | — |
| Product | Retinal | HCID 638015 | — |
Reaction Steps
Examples of the aldehyde of the general formula (1) include trimethylacetaldehyde, 2,2-dimethylbutanal, 2-ethyl-2-methylbutanal, 2,2-dimethyl-4-pentenal, 2,2-dimethylpentanal, 2,2-dimethylpenta-3,4-dienal and the like. Particularly, trimethylacetaldehyde (boiling point 74° C. at 730 mmHg) and 2,2-dimethy-4-pentenal (boiling point 124° C. at 760 mmHg) are preferable examples of the invention because the both substances themselves and the corresponding alcohols formed at the preparation of vitamin A aldehyde as side products have lower boiling points, so that these materials can be easily removed from the reaction mixtures at lower temperatures after the completion of the reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05087762 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-9dce8744d086419194eb3e2a210df7f1 |
| Source note | uspto-grants-1992_02 |