HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 7-Oxaspiro[3.5]nonane-6,8-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,2'-(Cyclobutane-1,1-diyl)diacetic acid | HCID 18704318 | — |
| Product | 7-Oxaspiro[3.5]nonane-6,8-dione | HCID 53438716 | 52.8% |
Reaction Steps
2,2′-(cyclobutane-1,1-diyl)diacetic acid (0.7 g, 4.07 mmol) was dissolved in acetic anhydride (5.75 mL, 61.0 mmol) and refluxed overnight. The solution was cooled to r.t. Acetic anhydride was removed under reduced pressure to give a brown oil, which was then recrystallized by dissolving in ether/hexanes, cooling to 0° C. and collecting crystals by vacuum filtration. The crystals were dried under vacuum overnight producing 7-oxaspiro[3.5]nonane-6,8-dione (2.147 mmol, 52.8% yield) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284283B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-e96fc88d5b2b4d42afd7444b499dc313 |
| Source note | uspto-grants-2016_03 |