HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554498Generated: October 26, 2026
Cuminaldehyde → (2-Benzyloxyphenyl)-(4-isopropylphenyl)methanol
https://huagongshe.com/reaction/554498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cuminaldehyde | HCID 326 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(Benzyloxy)-2-bromobenzene | HCID 561828 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Benzyloxyphenyl)-(4-isopropylphenyl)methanol | HCID 67459620 | 84% |
Reaction Steps
In a nitrogen stream, an n-butyllithium hexane solution (2.44 M, 5.14 mL) was added dropwise to a solution of 1-benzyloxy-2-bromobenzene (3.0 g, 11.4 mmol) in THF (114 mL) at −78° C. and the reaction mixture was stirred at the same temperature for 30 minutes. To this solution, a solution of 4-isopropylbenzaldehyde (1.41 g, 9.49 mmol) in THF (38 mL) was added dropwise at −78° C. The reaction mixture was stirred at the same temperature for one hour and furthermore at 0° C. for one hour. Water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:5)] to obtain the title compound (2.63 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08048897B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-f2976ad2a9a04cc49d3278293327f678 |
|---|
| Source note | uspto-grants-2011_11 |
|---|