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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398029Generated: October 29, 2026

Formaldehyde → Isobutyric anhydride

https://huagongshe.com/reaction/2398029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPivalolactoneHCID 16059—
ReactantHCID 54012568HCID 54012568—
ProductIsobutyric anhydrideHCID 7346—
ProductPivalolactoneHCID 16059—
ProductHCID 54012568HCID 54012568—

Reaction Steps

Following this procedure 50 milliliters of the catalyst from Example 1 is tested in continuous operation for four days. Formaldehyde conversion to pivalolacetone averages 68 percent with 14 percent going to isobutyroxypivalic anhydride, the product derived from the secondary reaction between pivalolactone, isobutyric acid and isobutyric anhydride. Isobutyric anhydride yield averages 66 percent to pivalolactone and 20 percent to isobutyroxypivalic anhydride. This catalyst is then regenerated by burning clean in air and steam at 550° C. and put back into service. For a similar four day period formaldehyde conversion to pivalolactone averages 74 percent with 8 percent going to isobutyroxypivalic anhydride. Isobutyric anhydride yield averages 76 percent to pivalolactone and 12 percent to isobutyroxypivalic anhydride. Another similar regeneration cycle is carried out and essentially the same results are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024080
Source datasetuspto-grants-1977_05
ORD IDord-4486171f872b40dab4c65f0a8a527311
Source noteuspto-grants-1977_05