HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 53973838, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | HCID 131710138 | HCID 131710138 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 53973838 | HCID 53973838 | 83.3% |
Reaction Steps
A mixture of 7.1 g of 2-acetoxyethyl-1,1-ethylenedioxy-2-n-pentyl-cyclopentane, 14.5 g of acetone and 0.0475 g of paratoluenesulphonic acid is brought to reflux during 1 hour. There is added thereto 0.08 mole of triethanolamine and the mixture is concentrated under reduced pressure on a water-bath. The residue is dissolved in 50 ml of benzene and washed with water until neutral. The distilled benzene solution yields 7 g of crude product which are rectified. There are obtained 5 g of 3-acetoxyethyl-2-n-pentyl-1-cyclopentanone (83.3% yield) having: b.p.0.5 = 110°-113°C, nD15 = 1.4610.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03981891 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-ed23227ce91a4e2fbd0e87ab00d4b3e8 |
| Source note | uspto-grants-1976_09 |