HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Acequinocyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178442823 | HCID 178442823 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acequinocyl | HCID 93315 | — |
Reaction Steps
A mixture of 2.0 parts of 2-n-dodecyl-3-hydroxy-1,4-naphthoquinone, 0.81 parts of triethylamine, 0.63 parts of acetyl chloride and 50 parts of methylene chloride was stirred at room temperature for 30 hours. The resulting mixture was distributed between methylene chloride and water. The methylene chloride layer was separated, dried over magnesium sulfate, then filtered and evaporated under reduced pressure. The residue was crystallized from petroleum ether (b.p. 30°-60°) to give 1.2 parts of 3-acetoxy-2-n-dodecyl-1,4-naphthoquinone, m.p. 57°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082848 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-09df9da89a424c0b8a3f2935a39077bf |
| Source note | uspto-grants-1978_04 |