HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (3-Bromo-2,6-difluorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Bromo-2,6-difluorobenzaldehyde | HCID 22139701 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromo-2,6-difluorophenyl)methanol | HCID 22219889 | 72.3% |
Reaction Steps
20 g of 3-bromo-2,6-difluorobenzaldehyde are dissolved in 450 ml of methanol and cooled in an ice bath; 3.42 g of sodium borohydride are then added portionwise thereto. The mixture is stirred at ambient temperature for 1 hour and then the solvent is evaporated 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 crystallised from n-pentane. 14.6 g of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148370B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-4b7cd46588334324b418e9a878fe6803 |
| Source note | uspto-grants-2012_04 |