HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391360Generated: October 27, 2026
Methanol → p-Isobutylpropiophenone dimethyl ketal
https://huagongshe.com/reaction/1391360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-(4-(2-Methylpropyl)phenyl)-1-propanone | HCID 108834 | — |
| Reactant | Ethanimidic acid, methyl ester, hydrochloride (1:1) | HCID 10313100 | — |
| Product | p-Isobutylpropiophenone dimethyl ketal | HCID 13298986 | — |
Reaction Steps
To 11.33 g. (0.10 mole) of methyl acetimidate hydrochloride, prepared by known methods, in a 100 ml. 3-necked, round bottom flask there was added a solution of 9.71 g. (actual 9.42 g.; 49.6 mmole) of crude p-isobutylpropiophenone, prepared as described in part A above, in 23 ml. of absolute methanol. The resulting solution was stirred for 12 hours at room temperature to insure complete reaction. Gas liquid chromatographic analysis (GLC analysis) of an aliquot of the reaction mixture indicated greater than 99% ketal formation. The resulting mixture was filtered to remove the precipitated ammonium chloride and concentrated under vacuum. Hexane (50 ml.) was added to the residue and the resulting solution was again filtered to remove any acetamide which might be present. Removal of the hexane solvent under vacuum gave p-isobutylpropiophenone dimethyl ketal as a pale yellow oil which was used without further purification. The NMR was in accord.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04142054 |
|---|
| Source dataset | uspto-grants-1979_02 |
|---|
| ORD ID | ord-99c328114f034f5e84c2b016ac8620e6 |
|---|
| Source note | uspto-grants-1979_02 |
|---|