HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → (1S,5R,6S)-6-Diethoxymethyl-2-oxabicyclo-[3,3,0]octan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (1S,5R,6S)-6-formyl-2-oxabicyclo[3,3,0]octan-3-one | HCID 12884327 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1S,5R,6S)-6-Diethoxymethyl-2-oxabicyclo-[3,3,0]octan-3-one | HCID 22813163 | — |
Reaction Steps
4.3 g. of (1S,5R,6S)-6-formyl-2-oxabicyclo-[3,3,0]octan-3-one [see Example 9(a)], 15 ml. of triethyl orthoformate, and 40 mg. of p-toluenesulfonic acid in 15 ml. of absolute ethyl alcohol are agitated for 16 hours at 20° under argon. The mixture is then diluted with ether, shaken in succession with sodium bicarbonate solution and water, dried over magnesium sulfate, and evaporated under vacuum, thus obtaining 4.8 g. of the title compound as an oil which is completely uniform as determined by thin-layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235930 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-37dd50195fec4e079b2d9d0d31cf8d35 |
| Source note | uspto-grants-1980_11 |