HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 178444439, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Pentylcyclohexanal | HCID 14085659 | — |
| Reactant | [3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide | HCID 18471791 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 178444439 | HCID 178444439 | — |
Reaction Steps
To a solution of [3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide 3D (R=pentyl) (1.68 g) in tert-butyl methyl ether at room temperature is added, dropwise, a 2.6 M solution of butyllithium (1.25 mL). The orange reaction mixture is stirred for 30 minutes, then a solution of cyclohexanal 3F (R=pentyl) (0.558 g) in tert-butyl methyl ether (3 mL) is added dropwise. The reaction is stirred a further 30 minutes, then poured into water and extracted with ether. The combined organic layers are washed with brine, then dried over sodium sulfate. The solvent is removed in vacuo and the residual material is flash chromatographed using 10% ethyl acetate in hexanes as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413448B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-d061030504034931b997d04d806f93a4 |
| Source note | uspto-grants-2002_07 |