HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 21273108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 21273100 | HCID 21273100 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21273108 | HCID 21273108 | — |
Reaction Steps
A mixture of 14.4 g of 1-(2-nonylphenyl)-1-hexanol, 2 g of toluene-4-sulphonic acid monohydrate and 250 ml of toluene is heated under reflux for 3 hours using a water separator. After cooling, the reaction mixture is washed twice with 10% strength (w/v) sodium bicarbonate solution and twice with water. The organic phase is dried over sodium sulphate and concentrated by evaporation in vacuo, and the residue is purified by chromatography on silica gel using hexane as eluant. The desired 1-(2-nonylphenyl)-transhexene is obtained in the form of a pale yellow oil. IR (CH2Cl2): 2960, 2930, 2855, 1465, 970 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04785004 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-5d4b7775a7684f0fb7f309bcc7fcea6a |
| Source note | uspto-grants-1988_11 |