HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (2E)-3-(4-bromophenyl)prop-2-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl trans-4-Bromocinnamate | HCID 688115 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2E)-3-(4-bromophenyl)prop-2-en-1-ol | HCID 11183465 | 100% |
Reaction Steps
To a solution of (E)-ethyl 3-(4-bromophenyl)acrylate (10.0 g, 39.2 mmol) in dichloromethane (151 mL) cooled to −78° C. was added a solution of diisobutylaluminum hydride (1.0 M in dichloromethane, 82 mL, 82 mmol) dropwise over 15 minutes time. The solution was then stirred for an additional 2 hours followed by the addition of a solution of 10% aqueous sodium hydroxide (250 mL). The mixture was allowed to warm to room temperature, and then the mixture was extracted with dichloromethane. The organic layer was dried and concentrated to afford 8.35 g (100%) of the title compound used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937150B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-1df2ed5218da463691bb152835a8ebce |
| Source note | uspto-grants-2015_01 |