HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Oxalate → HCID 68358222, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 2,2-Dimethoxycycloheptan-1-one | HCID 13167181 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 68358222 | HCID 68358222 | 65% |
Reaction Steps
1M LiN(TMS)2 in THF (28.5 mL, 28.5 mmol) were added dropwise at −50° C. to a solution of 2,2-dimethoxycycloheptanone (4.10 g, 23.8 mmol) in 25 mL of Et2O under argon. After 30 minutes at the same temperature, 3.55 mL of diethyloxalate were also added under stirring. The solution was kept at room temperature overnight. 10% solution of KH2PO4 (20 mL) were then added and the resulting solution extracted with Et2O (3×50 mL). The organic layer was dried over Na2SO4 and evaporated to dryness. The crude was purified by chromatography on a silica gel column (eluant: AcOEt/cyclohexane 1/9) to afford 3.98 g (65% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916577B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-88f058be812f4401b845c62790c489f8 |
| Source note | uspto-grants-2014_12 |