HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 2-(4-oxocyclohexyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 2-(1,4-dioxaspiro[4.5]decan-8-yl)acetate | HCID 20711792 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 2-(4-oxocyclohexyl)acetate | HCID 21249113 | 108.5% |
Reaction Steps
A 1 N aqueous hydrochloric acid solution (50 mL)/acetone (200 ml) mixture of (1,4-dioxa-spiro[4.5]dec-8-yl)-acetic acid methyl ester (4.99 g) obtained in Example (1b) was stirred at room temperature for 15 hours. The organic solvent was removed using an evaporator. The remaining aqueous solution was subjected to two extractions with ethyl acetate. The organic layer was washed with saturated brine, then dried over sodium sulfate, and then concentrated to obtain the title compound (4.30 g, quantitative yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735425B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-fb35a696927b494fbeb28c853f0474a5 |
| Source note | uspto-grants-2014_05 |