HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pinacolone → HCID 86735615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pinacolone | HCID 6416 | — |
| Reactant | Acetone, oxime | HCID 67180 | — |
| Reactant | tert-Butylglyoxal | HCID 349972 | — |
| Product | HCID 86735615 | HCID 86735615 | — |
Reaction Steps
Yet another oxime intermediate is prepared from t-butyl methyl ketone, which is first transformed into t-butylglyoxal using the procedure of Fuson et al., J. Am. Chem. Soc. 61, 1938 (1939). The t-butylglyoxal, in aqueous solution at pH 4-5, is allowed to react with acetone oxime (commercially available) at about room temperature for about two days. The reaction product mixture is worked up by extracting it with ether, and the t-butylglyoxal oxime is isolated from the ether extract as colorless needles having a melting point of about 50°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE030563 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-569ebd4f04804b7cb77c7aa2a324e21b |
| Source note | uspto-grants-1981_03 |