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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408108Erstellt: 25. Oktober 2026

Hydrogen Sulfide → 1,9-dimethyl-10H-phenothiazine

https://huagongshe.com/reaction/408108

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen SulfideHCID 402—
EduktIodineHCID 807—
EduktBenzenamine, 2-methyl-N-(2-methylphenyl)-HCID 136423—
EduktSulfurHCID 5362487—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt1,9-dimethyl-10H-phenothiazineHCID 6746449115%

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

To a reaction vessel were combined di(2-tolyl)amine (11.7 g, 59.3 mmol), elemental sulfur (3.9 g, 121.65 mmol, 2 eq.), crushed iodine (0.44 g, 1.73 mmol, 3 mol %) followed by o-dichlorobenzene (22 mL). Added an outlet to a dilute bleach solution (for hydrogen sulfide evolution) then put under argon. Refluxed at 180° C. for 4 h and removed solvent under reduced pressure. Purified by column chromatography with 2.0% ethyl acetate/98% hexane to obtain the desired product as white crystals (2 g, 8.8 mmol, 15% yield). Alternatively, the reaction was cooled to about 60° C. then hexane was added for extraction. Repeated hot hexane extractions of reaction until the product was no longer obtained in residue (about four times). Combined hexane extractions and concentrated in vacuo. Purified resulting residue either through repeated hot acetone/isopropanol crystallizations (or triturations) or flash column chromatography using 2% ethyl acetate/98% hexane to obtain product as white crystals (2.92 g, 12.8 mmol, 28% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759336B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-3176436d63ff43128bda32f193290546
Quellennotizuspto-grants-2014_06