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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614089Generated: October 30, 2026

Dichloromethane → Acequinocyl

https://huagongshe.com/reaction/614089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 178442823HCID 178442823—
SolventWaterHCID 962—
ProductAcequinocylHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143157
Source datasetuspto-grants-1979_03
ORD IDord-af645026134a479ea578d7cffb0043f6
Source noteuspto-grants-1979_03