HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2-(2-Benzyloxyethoxy)-cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Cyclohexanone, 2-hydroxy- | HCID 10785 | — |
| Reactant | Benzyloxyethanol | HCID 19595026 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(2-Benzyloxyethoxy)-cyclohexanone | HCID 20077960 | 67.1% |
Reaction Steps
A mixture of dimeric 2-hydroxycyclohexanone (13.7 g), 2 benzyloxyethanol (20 g) and p-toluensulphonic acid (2 g) were dissolved in xylene (500 ml) in a round bottom flask fitted with a Dean Stark apparatus and reluxed for 10 hrs. The resulting solution was cooled, washed with sodium hydrogen carbonate (3×50 ml) dried and concentrated under reduced pressure. The crude oil was then purified by flash chromatography using cyclohexane/ethyl acetate 60/40 as eluant yielding 20 g of the title compound (Rf=0.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05407931 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-465f23e0acd14dcb8bd9ce9fcb10622f |
| Source note | uspto-grants-1995_04 |