HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Methyl 2-(4-chlorophenyl)-3-methylbutanimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| Reactant | 2-(4-Chlorophenyl)-3-methylbutanamide | HCID 12898176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(4-chlorophenyl)-3-methylbutanimidate | HCID 20571405 | — |
Reaction Steps
To a mixture of 2.32 g (11 mmol) of 2-(4-chlorophenyl)-3-methylbutyramide in methylene chloride is added, at room temperature, 1.78 g (12 mmol) of trimethyloxonium tetrafluoroborate. After stirring overnight under nitrogen, the resulting solution is poured onto an ice-cold mixture of ether and aqueous sodium bicarbonate. The aqueous layer is discarded, and the ethereal layer is washed with cold water and dried over sodium sulfate. Filtration and concentration in vacuo affords methyl 2-(4-chlorophenyl)-3-methylbutanimidate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254264 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-d9de5dc4c3764659be7fd3d381ac650b |
| Source note | uspto-grants-1981_03 |