HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1,4-Di-[(methanesulfonyl)oxy]-2-(hydroxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2.5-Di-[(methanesulfonyl)oxy]benzaldehyde | HCID 18536186 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 1,4-Di-[(methanesulfonyl)oxy]-2-(hydroxymethyl)benzene | HCID 18536045 | — |
Reaction Steps
To a solution of the product from Step A (17.13 g, 58.2 mmol) in 150 mL of 2:1 THF/ethanol at 0° C. was added sodium borohydride (2.27 g, 60.0 mmol). After 30 minutes, the reaction was carefully quenched by the addition oc saturated NH4Cl solution, then partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with water and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The product was isolated as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562823B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-af8b38658e2845c38b40455500b14b75 |
| Source note | uspto-grants-2003_05 |