HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(4-Tert-butylphenyl)-2-(3-chloropropyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4'-tert-Butyl-4-chlorobutyrophenone | HCID 2723694 | — |
| Reactant | Diethylether heptane | HCID 21897273 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Tert-butylphenyl)-2-(3-chloropropyl)-1,3-dioxolane | HCID 22320900 | — |
Reaction Steps
This compound was synthesized as described under 5.a) with 20.0 g (83.8 mmol) of 1-(4-tert-butylphenyl)-4-chloro-1-butanone (origin: Acros), 16 ml of ethylene glycol and ca. 1 g of p-toluenesulfonic acid in 120 ml of toluene for 16 h to give 24.1 g (99%) of the crude compound, which was used for further functionalization. Column chromatography of 3 g (SiO2, heptane/ether 4:1) afforded 2.48 g of a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06949680B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-1364835ed6ea41f380a92199589e008c |
| Source note | uspto-grants-2005_09 |