HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3-nitrobenzaldehyde → 4-Chloro-3-nitrobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3-nitrobenzaldehyde | HCID 85505 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Chloro-3-nitrobenzyl alcohol | HCID 91933 | — |
Reaction Steps
To a solution of 4-chloro-3-nitrobenzaldehyde (5.0 g, 27 mmol) in EtOH (100 mL) at rt was added portion wise NaBH4 (1.02 g, 1 eq). The mixture was stirred at RT for 2 h, concentrated in vacuo and partitioned between ether and water. The organic layer was washed with brine, dried over MgSO4 and concentrated. The title alcohol was recovered as a brownish solid (4.96 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003654B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-06219b42ac7945fa9e786bb18503fecf |
| Source note | uspto-grants-2011_08 |