Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534274Generated: November 4, 2026

Pivalaldehyde → Retinal

https://huagongshe.com/reaction/1534274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
Reactant2,2-Dimethyl-3,4-pentadienalHCID 77678—
Reactant2,2-Dimethylpent-4-enalHCID 79636—
Reactant2,2-DimethylvaleraldehydeHCID 84292—
ReactantButanal, 2,2-dimethyl-HCID 137426—
ReactantHCID 15174357HCID 15174357—
ProductRetinalHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087762
Source datasetuspto-grants-1992_02
ORD IDord-9dce8744d086419194eb3e2a210df7f1
Source noteuspto-grants-1992_02