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HRID 408108作成日:2026年10月25日

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

https://huagongshe.com/reaction/408108

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen SulfideHCID 402—
反応物IodineHCID 807—
反応物Benzenamine, 2-methyl-N-(2-methylphenyl)-HCID 136423—
反応物SulfurHCID 5362487—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物1,9-dimethyl-10H-phenothiazineHCID 6746449115%

反応条件

温度180 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759336B2
出典データセットuspto-grants-2014_06
ORD IDord-3176436d63ff43128bda32f193290546
出典メモuspto-grants-2014_06