HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-(2H-1,2,3-Triazol-2-yl)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(2H-1,2,3-triazol-2-yl)benzaldehyde | HCID 10797302 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2H-1,2,3-Triazol-2-yl)benzenemethanol | HCID 21943696 | — |
Reaction Steps
To a solution of 42.26 g (244 mmol) of 4-[1,2,3]-triazol-2-yl-benzaldehyde in 140 ml of THF and 420 ml of MeOH, 9.23 g (244 mmol) of NaBH4 are added portionwise at 0–5° C. and the mixture is stirred for 30 min. at the same temperature. The reaction is quenched with sat. NH4Cl at 0–5° C. and the mixture is extracted with AcOEt. The combined extracts are washed with brine, dried over MgSO4 and concentrated under reduced pressure to give the title compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112611B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-936aa10a07a04a97a4a814eeef6d73b9 |
| Source note | uspto-grants-2006_09 |