HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexanoyl chloride → HCID 13912741, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | HCID 70431917 | HCID 70431917 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 13912741 | HCID 13912741 | — |
Reaction Steps
The subject compound was prepared by reaction of 5-(1-methylethyl)-2-(3,5,6-trimethyl-2-pyrazinyl)-1,3-cyclohexanedione potassium salt (Example 8) with hexanoyl chloride employing the general procedure described in Example 3, but allowing the reaction mixture to stir at room temperature over the weekend. Following the reaction, the ether solution of crude product was extracted quickly with ice-cold 0.25N NaOH, dried (MgSO4), filtered and evaporated to give a residue product showing some acid chloride contamination by IR examination. Dry-column chromatography using 1:1 ethyl acetate/hexane gave analytically pure material as shown by the elemental analysis of Table II.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04678501 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-3c4e68c39c7e40ea8c15f66945e4c1d8 |
| Source note | uspto-grants-1987_07 |