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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419775Generated: November 2, 2026

Dichloromethane → Acequinocyl

https://huagongshe.com/reaction/2419775

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-1,4naphthoquinone 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 numberUS04107325
Source datasetuspto-grants-1978_08
ORD IDord-57c4e198bdb5417b9ef12296f68b618e
Source noteuspto-grants-1978_08