HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → methyl 5-formyl-(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-pentanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | methyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-6-heptenoate | HCID 86743990 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | methyl 5-formyl-(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-pentanecarboxylate | HCID 86743989 | — |
Reaction Steps
A solution of 2.56 g of methyl (R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-6-heptenoate in 40 ml of ethyl acetate is treated with ozone at -75° C. After the reaction has finished 0.1 g of Pd-on-carbon is added thereto and the mixture is hydrogenated at room temperature. After the hydrogen uptake has finished one filters off the catalyst, washes with ethyl acetate and evaporates in vacuo. There is obtained crude methyl 5-formyl-(R)-3-[(tetrahydro-2H-pyran-2-yl)oxy]-pentanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983746 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-5d9d0b90eb424adb83865c33781a2d11 |
| Source note | uspto-grants-1991_01 |