HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anisole → 18-(p-Iodophenyl)octadecanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-Benzyloxy-18-(p-iodophenyl)octadecane | HCID 18471597 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 18-(p-Iodophenyl)octadecanol | HCID 11655804 | — |
Reaction Steps
Finally, to a solution of 1-benzyloxy-18-(p-iodophenyl)octadecane (Compound V) (185 mg; 0.33 mmol) and anisole (0.15 ml; 1.32 mmol) in dichloromethane (3 ml) was added anhydrous aluminum chloride (135 mg; 1 mmol) at the room temperature. Stirring was continued for 2 h. The reaction was quenched by diluted hydrochloric acid and extracted by chloroform. Extract was dried (Na2SO4) and evaporated. The residue was chromatographed in hexane-ethyl acetate (gradient from 95:5 to 85:15) to give 18-(p-iodophenyl) octadecanol, Compound VI (123 mg; 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06255519B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-54e0b1ce383743008d3153e25f6a14f2 |
| Source note | uspto-grants-2001_07 |