HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanone, 1-(3-phenoxyphenyl)- → 1-(3-Phenoxyphenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanone, 1-(3-phenoxyphenyl)- | HCID 36249 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | 1-(3-Phenoxyphenyl)ethanol | HCID 12882419 | — |
Reaction Steps
m-Phenoxyacetophenone is reduced with sodium borohydride to form alpha-(m-phenoxyphenyl)ethyl alcohol which is then reacted with phosphorus tribromide to form alpha-(m-phenoxyphenyl)ethyl bromide. This product is reacted with sodium cyanide under heat in dimethyl sulfoxide. Hydrolysis of the product with sodium hydroxide gives the desired alpha-(m-phenoxyphenyl)propionic acid. (For details, see U.S. Pat. No. 3,600,437).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04340740 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-5bf6ec19a67c4957ab80a2777e68908a |
| Source note | uspto-grants-1982_07 |