HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Pentylcyclohexanal → 2-Benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Pentylcyclohexanal | HCID 14085659 | — |
| Reactant | (6-Benzyloxynaphthalen-2-ylmethyl)-triphenyl-phosphonium Bromide | HCID 20632177 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-Benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthalene | HCID 69884788 | 74% |
Reaction Steps
The solution of (6-benzyloxy-naphthalen-2-ylmethyl)-triphenyl-phosphonium bromide (19) (1 equi.), 4-pentyl-cyclohexanecarboxaldehyde (22), and potassium tert-butoxide (1.3 equi.) in tert-butyl methyl ether (6 mL/mmole) was stirred at room temperature for 24 h, then quenched with water, extracted with diethyl ether, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (1.25% EtOAc/hexane) afforded 2-benzyloxy-6-[2-(4-pentyl-cyclohexyl)-vinyl]-naphthalene (23) as a white solid (74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703082B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-f6c63d21095849468799f3cf0417b9fa |
| Source note | uspto-grants-2004_03 |