HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenoxyacetyl chloride → HCID 53690513, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenoxyacetyl chloride | HCID 69703 | — |
| Reactant | Isoproterenone hydrochloride | HCID 2830496 | — |
| Product | HCID 53690513 | HCID 53690513 | — |
Reaction Steps
Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and phenoxyacetyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(phenoxyacetoxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is catalytically hydrogenated, using a procedure similar to that described above in Example 2B, there is obtained 3-hydroxy-4-(phenoxyacetoxy)-alpha-(isopropylaminomethyl)benzyl alcohol methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04336400 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-8d10ca0cf045458aac95ffa20d37d498 |
| Source note | uspto-grants-1982_06 |