HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Isobutyric anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Pivalolactone | HCID 16059 | — |
| Reactant | HCID 54012568 | HCID 54012568 | — |
| Product | Isobutyric anhydride | HCID 7346 | — |
| Product | Pivalolactone | HCID 16059 | — |
| Product | HCID 131710747 | HCID 131710747 | — |
Reaction Steps
This example shows the lower yields and conversions obtained by the usually prepared tantalum oxide on silica gel catalyst. The catalyst is prepared by the same procedure described in Example 1 except that after treatment in air at 550° C. for 1.5 hours the reactor is cooled and put into service. This material is not steam treated at high temperatures. The catalyst is tested as described in Example 2 in continuous operation for two days. For this period formaldehyde conversion to pivalolactone averages 28 percent with 26 percent going to isobutyroxypivalic anhydride. Isobutyric anhydride yield for the same two days averages 30 percent to pivalolactone and 41 percent to isobutyoxypivalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024080 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-486d7dcb321b43b6a6693908d1a5d7e8 |
| Source note | uspto-grants-1977_05 |