HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-Acetoxy-2-naphthoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Hydroxy-4-naphthoic acid | HCID 344291 | — |
| Reactant | Acetoxy carboxylic acid | HCID 17769302 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Acetoxy-2-naphthoic acid | HCID 20074592 | — |
Reaction Steps
To a suspension of 2.3 g. of 4-hydroxy-1-naphthoic acid in 100 ml. of methylene chloride and 100 ml. of tetrahydrofuran, a mixture of 1.5 g. of triethylamine, 1.6 g. of 4-N-dimethylaminopyridine and 1.5 g. of acetic anhydride is added. The reaction mixture is heated at 50° for one hour. The solution is extracted with ethyl acetate, the organic layer washed with water and dilute hydrochloride acid and evaporated to dryness to yield 2.1 g. of the acetoxy carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04145443 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-d13c83f37c464df289808309d006fe33 |
| Source note | uspto-grants-1979_03 |