HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenolate Sodium → 3-(3,3-Dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenolate Sodium | HCID 4445035 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Neoheptanoyl chloride | HCID 14921487 | — |
| Reactant | 3-Hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone | HCID 54189973 | — |
| Product | 3-(3,3-Dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone | HCID 54114160 | — |
Reaction Steps
Following a procedure similar to that described in Example 2A above, when 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is interacted with 3,3-dimethylbutanecarbonyl chloride there is obtained 3-(3,3-dimethylbutanecarbonyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone which reacts with hydrochloric acid to yield the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using the procedure described above in Example 2B, there is obtained 3-(3,3-dimethylbutanecarbonyloxy)-4-(p-toluyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336400 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-1e193545b1a2464cb2f2dec0bd88387a |
| Source note | uspto-grants-1982_06 |