HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-Fluoro-3-nitrobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Fluoro-3-nitrobenzaldehyde | HCID 598129 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Fluoro-3-nitrobenzyl alcohol | HCID 4167587 | 103.7% |
Reaction Steps
Sodium borohydride (1.36 g, 35.95 mmol) was added to a solution of 4-fluoro-3-nitrobenzaldehyde (2.0 g, 11.83 mmol) in methanol (15 mL) and water (3.0 mL), and the mixture was stirred at room temperature for 3 hours. Water was then added to the reaction mixture, and extraction was performed with ethyl acetate. The organic extract was washed with saturated saline and dried over magnesium sulfate, and then concentrated under reduced pressure to yield the title compound (2.10 g, 95%) as a pale red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897792B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-e1f1f5224c1e42da9c57b7e740b67605 |
| Source note | uspto-grants-2011_03 |