HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-cyclohexylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Cyclo-hexylpropionate | HCID 22016473 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 2-cyclohexylpropionate | HCID 160641 | 96% |
Reaction Steps
Into a 500 ml round bottom flask equipped with a Soxhlet extractor filled with molecular sieves, 50 g of 2-cyclo-hexylpropionate, 100 g of ethanol, 0.5 g of p-toluene sulfonic acid, and 200 ml of chloroform were charged. The mixture was reacted under refluxing for 40 hours. The reaction mixture was washed with water and distilled under reduced pressure to obtain 56.4 g of ethyl 2-cyclohexylpropionate (yield: 96%, purity: 99.4%). The compound obtained had a fruity (namely aldehyde C-16 and apple-like) odor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05049544 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-abc26ddb0e7c40968d2fa53c257c1ac0 |
| Source note | uspto-grants-1991_09 |