HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-Bromo-6-fluorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Bromo-6-fluorobenzaldehyde | HCID 22473977 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2-Bromo-6-fluorophenyl)methanol | HCID 44181801 | 89.6% |
Reaction Steps
20.0 g (0098 mol) of 2-bromo-6-fluorobenzaldehyde are dissolved in 500 ml of methanol and cooled in an ice bath; 3.72 g (0.098 mol) of sodium borohydride are then added thereto, portionwise. The mixture is stirred under cold conditions for 1 hour and the solvent is then evaporated off under reduced pressure. The residue is taken up between water and dichloromethane, and the organic phase is separated, dried and concentrated under reduced pressure. The residue is crystallized from pentane. 18.1 g of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338451B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-3b776c9206ec4bdf9851abee129f4ea4 |
| Source note | uspto-grants-2012_12 |