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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26236Generated: October 30, 2026

Acetyl chloride → 3-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone

https://huagongshe.com/reaction/26236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178442826HCID 178442826—
SolventDichloromethaneHCID 6344—
Product3-Acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinoneHCID 21325243—

Reaction Steps

A solution of 0.95 parts of 5-chloro-2-dodecyl-3-hydroxy-1,4-naphthoquinone in 20 parts of anhydrous tetrahydrofuran was added under nitrogen to a mixture of 0.0635 parts of dispersed sodium hydride in 40 parts of tetrahydrofuran with stirring at room temperature. After 45 minutes of stirring, a solution of 0.275 parts of acetyl chloride in 30 parts of tetrahydrofuran was added and the mixture stirred for 5 hours. The tetrahydrofuran was stripped under reduced pressure and the residue taken up in methylene chloride and then washed with water, 10% hydrochloric acid, four more times with water, dried over sodium sulfate and stripped. The resulting yellow solid was purified by column chromatography on silica gel using 1-chlorobutane as eluent. Solvent removal gave 0.9 parts of 3-acetoxy-5-chloro-2-dodecyl-1,4-naphthoquinone, m.p. 57°-59° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148918
Source datasetuspto-grants-1979_04
ORD IDord-a23e3a8557d14704af10c6d5c0d72db7
Source noteuspto-grants-1979_04