HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenolate Sodium → HCID 54364113, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenolate Sodium | HCID 4445035 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 14696615 | HCID 14696615 | — |
| Reactant | HCID 20535365 | HCID 20535365 | — |
| Product | HCID 54364113 | HCID 54364113 | — |
Reaction Steps
Following a procedure similar to that described in Example 30A above, when 3-hydroxy-4-(7,7-dimethyloctanoyloxy)-phenyl tert-butylaminomethyl ketone is interacted with one equivalent of sodium methoxide and the resulting sodium phenolate salt is reacted with p-isopropoxyphenylacetyl chloride there is obtained 3-(p-isopropoxyphenylacetoxy)-4-(7,7-dimethyloctanoyloxy)phenyl tert-butylaminomethyl ketone which reacts with methanesulfonic acid to yield the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using the procedure described above in Example 30B, there is obtained 3-(p-isopropoxyphenylacetoxy)-4-(7,7-dimethyloctanoyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336400 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-c9ddcbdba78b4955892a121b1b2a7ab9 |
| Source note | uspto-grants-1982_06 |