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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660168Generated: October 27, 2026

Dichloromethane → 5-Cyano-1-(2,6-dimethylphenyl)-3-(1,1,2,2-tetrachloroethanesulfenyl)uracil

https://huagongshe.com/reaction/1660168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,1,2,2-Tetrachloroethylsulfenyl chlorideHCID 14453—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13014421HCID 13014421—
SolventWaterHCID 962—
Product5-Cyano-1-(2,6-dimethylphenyl)-3-(1,1,2,2-tetrachloroethanesulfenyl)uracilHCID 13093904—

Reaction Steps

To an ice cold solution of 1.60 g (0.04 mol) of NaOH in 45 ml of water is added 9.64 g (0.04 mol) of 5-cyano-1-(2,6-dimethylphenyl)uracil, obtained as in Example 1. After dissolution, 50 ml of ice cold dichloromethane is added, followed by a solution of 9.36 g (0.04 mol) of 1,1,2,2-tetrachloroethanesulphenyl chloride (prepared by the method of U.S. Pat. No. 3,395,180) in 15 ml. of dichloromethane. The mixture is stirred for 30 min at 4°. The aqueous layer is separated and discarded. The dichloromethane solution is dried and stripped at aspirator pressure. The unreacted sulphenyl chloride is then removed by trituration with pentane/dichloromethane (4:1). The resultant crude product is purified by slurrying at 30° in 60 ml of ethanol-free chloroform, allowed to cool to RT and filtered. To the filtrate is added hexane to the cloud point, and the mixture is then filtered to yield 5-cyano-1-(2,6-dimethylphenyl)-3-(1,1,2,2-tetrachloroethanesulphenyl)uracil, m.p. 180°-183°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307098
Source datasetuspto-grants-1981_12
ORD IDord-310512753cfe42359de2aae1ed7aafc9
Source noteuspto-grants-1981_12