HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 15044964, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15044963 | HCID 15044963 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15044964 | HCID 15044964 | 98.1% |
Reaction Steps
15.5 g (0.065 mole) of 3-methoxy-5-methylthio-4-propoxybenzaldehyde in 300 ml of methanol was cooled in ice bath. 1 g (0.026 mole) of sodium borohydride was added in 3 portions to the above solution. The mixture was stirred for 10 minutes in ice bath. MeOH was removed, and the residue was purified by flash column chromatography to afford 15.45 g (95% yield) of 3-methoxy-5-methylthio-4-propoxybenzyl alcohol as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05132463 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-89845acfe9964b3c8a5dbdd60e970c1b |
| Source note | uspto-grants-1992_07 |