HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 15718590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12231028 | HCID 12231028 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15718590 | HCID 15718590 | — |
Reaction Steps
The compound obtained in step (iii) above (16.2 g, 0.080 mol) is reduced with sodium borohydride (3.1 g, 0.082 mol) in absolute methanol (500 ml). The reaction mixture is concentrated under vacuum, ice-water is added thereto, the mixture is made acidic by the addition of concentrated hydrochloric acid and extracted with ethyl acetate. Upon evaporation of the solvent 2-cyano-5-methoxy-1,2,3,4-tetrahydro-1-naphthol (16.2 g) is obtained; m.p. 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130339 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-75ef0e66fb554c3d8fa520277dc76cb0 |
| Source note | uspto-grants-1992_07 |