HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (2-Bromo-5-ethoxy-4-methylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 2-Bromo-5-ethoxy-4-methylbenzoate | HCID 86676806 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2-Bromo-5-ethoxy-4-methylphenyl)methanol | HCID 66764839 | 100.6% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 2-bromo-5-ethoxy-4-methylbenzoate (660 mg, 2.23 mmol) in ether (20 mL) at 0° C. was added DIBAL (5.75 mL, 5.75 mmol, 1 M in toluene). The reaction was stirred at 0° C. for 10 minutes. EtOAc (20 mL) and wet silica gel (˜50 g silica gel and 3 mL of water) were added portion wise at 0° C. The resulting slurry was stirred for ˜15 minutes and was filtered, washed with EtOAc (20 mL). The organic phase was dried over sodium sulfate, filtered and concentrated. The residue was purified on a silica gel column eluting with EtOAc/hexanes (20/80) to give the title intermediate (550 mg) as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742110B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-13f7f37a386f4f338cfb418d935bb65f |
| Source note | uspto-grants-2014_06 |