HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 1-(2-Iodoethyl)-4-octylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4'-(2-Iodoethyl)octanophenone | HCID 11132076 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1-(2-Iodoethyl)-4-octylbenzene | HCID 10545362 | — |
Reaction Steps
To a solution of 4′-(2-iodoethyl)octanophenone (200 g) in trifluoroacetic acid (319 ml) is added triethylsilane (195.7 ml) under ice-cooling, and the mixture is stirred at room temperature for 2 hr. The reaction mixture is concentrated, and the residue is distilled away under reduced pressure to give the title compound (7) as a pale-red oil. The resulting Compound (7) has the same physico-chemical characteristics as indicated in Example 15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605744B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-100ce2bbc30a4158acd12bce979447fb |
| Source note | uspto-grants-2003_08 |