HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 14722249, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14722248 | HCID 14722248 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 14722249 | HCID 14722249 | — |
Reaction Steps
A solution 5.0 g of 4-(cyclohexylamino)-1-acetoxy-2-methoxynaphthalene in 75 ml of acetic anhydride is stirred with 500 mg of zinc chloride in at 160°-170° C. for 2 hours. The reaction is cooled, filtered and evaporated under reduced pressure. The residue is taken up in 300 ml of diethyl ether and washed with 100 ml of water and then with 100 ml of brine. The organic solvent is dried over magnesium sulfate, filtered, and evaporated to dryness. The residue is crystallized from 120 ml of 2:1 diethyl ether-hexane to yield 4-(N-acetylcyclohexylamino)-1-acetoxy-2-methoxynaphthalene, m.p. 137°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04882339 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-563818c3657a4d0ca235bb9d8641c5ad |
| Source note | uspto-grants-1989_11 |