HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-Hydroxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Methoxy-2-naphthyl-2-methylsulfonyloxy-1-propanone | HCID 13231055 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Hydroxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate | HCID 13713538 | — |
Reaction Steps
Representative of Scheme III is the reaction of 1-(6-methoxy-2-naphthyl)-2-methanesulfonyloxypropan-1-one with sodium borohydride in methanol to yield 1-hydroxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate. Treating that material with sodium acetate in acetic acid affords 2-(6-methoxy-2-naphthyl)propanal, which is oxidized with sodium chlorite to 2-(6-methoxy-2-naphthyl)propionic acid. By employing the optically active (S) 1-(6-methoxy-2-naphthyl)-2-methanesulfonyloxypropan-1-one there is obtained, following the same sequential steps, (S) 2-(6-methoxy-2-naphthyl)propionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04605758 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-6165992b19604d778243bd7b1461290b |
| Source note | uspto-grants-1986_08 |