HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 22800352, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | 7-[(3R)-3-Hydroxy-5-oxocyclopent-1-en-1-yl]heptanoic acid | HCID 16213149 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22800352 | HCID 22800352 | — |
Reaction Steps
To a solution of 1.70 parts of 7-(3(R)-hydroxy-5-oxocyclopent-1-en-1-yl)heptanoic acid in 12 parts by volume of dry benzene is added 0.005 part of p-toluenesulfonic acid and 3.40 parts of dihydropyran. The reaction mixture is allowed to stand at room temperature for about 24 hours. The resulting solution is diluted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate, and stripped of solvent under reduced pressure to afford tetrahydropyran-2-yl 7-(3(R)-tetrahydropyran-2-yloxy-5-oxocyclopent-1-en-1-yl)-heptanoate. This compound is represented by the following structural formula. ##STR21##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04060691 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-f22df2552fc84a519155c4d63e6b4c1d |
| Source note | uspto-grants-1977_11 |