HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Octyl-2,4,6-trimethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Mesitylene | HCID 7947 | — |
| Reactant | 1-Chlorooctane | HCID 8142 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Octyl-2,4,6-trimethylbenzene | HCID 19963886 | 34.7% |
Reaction Steps
A 750 ml flask is charged with 6.7 g (50 mmol) of anhydrous aluminium chloride and 120.2 g (1 mol) of mesitylene. 148.7 g (1 mol) of 1-chloroctane are added dropwise to this mixture over 2 h at room temperature. HCl gas slowly evolves. The dark orange emulsion is stirred for c. 30 h at room temperature and then poured into water and extracted with toluene. The organic phase is isolated and concentrated on a rotary evaporator. The resultant oil is fractionated under vacuum to give, at 88°-92° C. and 1.8 mbar, 80.6 g of the title product as a colourless liquid. Gas chromatography (GC) and 1H-NMR spectrum analysis show that mono-n-octylmesitylene is obtained in 90% purity. The distillation residue contains mainly dioctylmesitylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616787 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-5aec6e135de84d3e8073ee25308a0747 |
| Source note | uspto-grants-1997_04 |