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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23387Erstellt: 23. Oktober 2026

Dimethyl Sulfide → 2-Chloro-6-methylsulfanylmethyl-phenylamine

https://huagongshe.com/de/reaction/23387

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfideHCID 1068—
Edukt2-ChloroanilineHCID 7240—
EduktTriethylamineHCID 8471—
EduktChlorosuccinimideHCID 31398—
Lösungsmittel1,1-DichloroethaneHCID 6365—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Chloro-6-methylsulfanylmethyl-phenylamineHCID 32670982%

Reaktionsschritte

2-Chloro-phenylamine (12.76 g, 0.1 mole) and dimethyl sulfide (10 ml) were dissolved in dichloroethane (200 ml) and cooled in an ice-acetone-salt bath under a nitrogen atmosphere. N-chlorosuccinimide (14.70 g, 0.11 mole) dissolved in dichloroethane (300 ml) was slowly added via addition funnel over about 20-30 minutes. After stirring an hour beyond addition while allowing the reaction to reach room temperature, triethyl amine (30 ml) was added and the mixture was brought to reflux for 1 h and 20 minutes. The reaction was monitored by tlc (15:85 EtOAc:hexane on silica gel) which showed a single less polar product. The mixture was cooled and evaporated to dryness. The residue was taken up in methylene chloride, dry packed on silica gel, and placed onto a column of flash silica gel. The product was eluted from the column with 1:9 ethyl acetate:hexane to give 15.4 g of a homogeneous oil (82%), 2-chloro-6-methylsulfanylmethyl-phenylamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852726B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-33e3ac922d8e4f8d978a1b211f1d4a44
Quellennotizuspto-grants-2005_02