HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Hydroxy-3-(2-chlorophenylthio)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Hydroxy-3-(2-chlorophenylthio)benzaldehyde | HCID 20513443 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Hydroxy-3-(2-chlorophenylthio)benzyl alcohol | HCID 53931639 | 102.7% |
Reaction Steps
To a suspension of 2-hydroxy-3-(2-chlorophenylthio)benzaldehyde (5.8 g) in methanol (50 ml) was added sodium borohydride (820 mg) at temperature below 15° C. with stirring. The mixture was treated in a similar manner to that of Example 21-(5) to give oily 2-hydroxy-3-(2-chlorophenylthio)benzyl alcohol (6 g). This oily substance was left to stand at room temperature to give crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367238 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-895029dd627b4737bb6850571508fba6 |
| Source note | uspto-grants-1983_01 |