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 | 70.2% |
Reaction Steps
A mixture of 24.5 g of the 2-(1-naphthylmethylene)succinic acid obtained and 260 ml of acetic anhydride was heated for 60 minutes at 60° C. The reaction mixture was evaporated under reduced pressure, and to the residue was added a mixture of benzene and hexane (1:1). Precipitated crystals were collected by filtration to obtain 16.0 g of 2-(1-naphthylmethylene)succinic anhydride as orange yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04853463 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-7588cc9358094d0db8579e10a5532518 |
| Source note | uspto-grants-1989_08 |