HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 69907470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 22718777 | HCID 22718777 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 69907470 | HCID 69907470 | 42.9% |
Reaction Steps
To a solution of ethyl 3-hydroxy-3-(4′-cycloheptylphenyl)-butanoate (2c, 28.75 g) in benzene (175 ml) was added p-toluenesulfonic acid and was refluxed for 1 h. The reaction mixture was diluted with NaHCO3 and benzene layer was separated out. The organic layer was washed with water, dried (Na2SO4) and concentrated. The crude product was purified by column chromatography on silica gel to give 11.6 g (42.9% yield) of ethyl 3-(4′-cycloheptylphenyl)-but-2-enoate (3c, formula 3, R=cycloheptyl) as viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06737438B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-19269e2e21b14ed28fbf30e5aa705ec9 |
| Source note | uspto-grants-2004_05 |