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
A mixture of 7.6 g of 2-(1-naphthylmethylene)succinic acid obtained and 130 ml of acetic anhydride was heated under reflux for 1 hour. The reaction mixture was concentrated under reduced pressure, and 50 ml of benzene was added to the residue. The precipitated crystals were collected by filtration to obtain 3.4 g of 2-(1-naphthylmethylene)succinic anhydride as orange yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863904 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-ea6366dbeeb34046810d7304d03bf657 |
| Source note | uspto-grants-1989_09 |