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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118415Generated: November 2, 2026

Hexanoyl chloride → HCID 13912741, compound

https://huagongshe.com/reaction/2118415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanoyl chlorideHCID 67340—
ReactantHCID 70431917HCID 70431917—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 13912741HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678501
Source datasetuspto-grants-1987_07
ORD IDord-3c4e68c39c7e40ea8c15f66945e4c1d8
Source noteuspto-grants-1987_07