HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nicotinoyl chloride → 3-(Nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nicotinoyl chloride | HCID 82604 | — |
| Reactant | 3-Hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone | HCID 54189973 | — |
| Product | 3-(Nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone | HCID 53663371 | — |
Reaction Steps
Following a procedure similar to that described above in Example 30A, when 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone is interacted with nicotinoyl chloride, there is obtained 3-(nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone; and by interaction of this base with hydrochloric acid there is obtained the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using the procedure described above in Example 30B, there is obtained 3-nicotinoyloxy-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-e9fdb80045194a9db7152a23be254b48 |
| Source note | uspto-grants-1982_06 |