HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[(Naphthalen-1-yl)methylidene]butanedioic acid → 3-[(Naphthalen-1-yl)methylidene]oxolane-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[(Naphthalen-1-yl)methylidene]butanedioic acid | HCID 54142689 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 3-[(Naphthalen-1-yl)methylidene]oxolane-2,5-dione | HCID 54316428 | 48.1% |
Reaction Steps
To 260 ml of acetic anhydride was added 15.20 g of 2-(1-naphthylmethylene)succinic acid, and the mixture was heated under reflux for 1 hour. The reaction mixture was evaporated under reduced pressure, and 100 ml of dry benzene was added to the residue. The precipitated crystals were collected by filtration to obtain 6.80 g of 2-(1-naphthylmethylene)succinic anhydride as orange yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04841067 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-aef5bb294bb34c08af002acbb794ed33 |
| Source note | uspto-grants-1989_06 |