HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (2E)-2-(4-Bromophenyl)-3-cyclohexylprop-2-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | (E)-2-(4-Bromophenyl)-3-cyclohexylacrylic acid | HCID 53471257 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2E)-2-(4-Bromophenyl)-3-cyclohexylprop-2-en-1-ol | HCID 67084617 | 98.4% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
Add DIBAL in toluene (673 mL, 1.0 M, 673 mmol) to a solution of (E)-2-(4-bromo-phenyl)-3-cyclohexyl-acrylic acid (52 g, 168 mmol) in toluene (1.6 1) maintained at −78° C. Then allow the reaction mixture to slowly warm to room temperature, and stir, it for 18 h. Cool reaction mixture to 0° C. and add MeOH to destroy excess amounts of DIBAL. Add Rochelle's salt (100 mL) and HCl (2 N). Separate the layers and wash the organic layer with brine. Filter through hydrophobic filter and concentrate to obtain the title compound (48.8 g) as a white solid. MS (m/e): 277 (M+H−H2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576108B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-bdacf65e8f8b43818d7fe337e73943f3 |
| Source note | uspto-grants-2009_08 |