HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → HCID 54532739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70553942 | HCID 70553942 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54532739 | HCID 54532739 | — |
Reaction Steps
Proceeding in a manner similar to that described above in part B of Example 151, 22 g. of 3-(acetoxymethyl)-4-(o-toluyloxy)phenyl tert-butylaminomethyl ketone hydrochloride was reduced in anhydrous methyl alcohol with 1.13 g. of sodium borohydride and the reduction product was treated with methanesulfonic acid to yield 3-(acetoxymethyl)-4-(o-toluyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol methanesulfonate as a white solid which melted at 116-118° C.(uncorr.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138581 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-5bb12550404849c2bbfe0f66fd3d273f |
| Source note | uspto-grants-1979_02 |