HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 71170040, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(Furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-one | HCID 71170035 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71170040 | HCID 71170040 | — |
Reaction Steps
1-(Furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-one (4 kg, 13.69 mol) was dissolved in MeOH (35 L), and NaBH4 (520 g, 13.75 mol) was slowly added to the solution at 5° C. After the reaction was completed, the solution was quenched with H2O, and the MeOH was evaporated. The residue was extracted with EtOAc and the organic layer was washed with brine, dried over MgSO4, and evaporated to give the 1-(furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-ol as yellow oil: 3.97 kg (crude yield: 98%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08350090B1 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-b67e4372c76d47dfb1b43c3c7b854972 |
| Source note | uspto-grants-2013_01 |