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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 892786Erstellt: 24. Oktober 2026

Triethylamine → 2-(Dimethylamino)methyl-3-methylthiophene

https://huagongshe.com/de/reaction/892786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktThionyl ChlorideHCID 24386—
Edukt(3-Methylthiophen-2-yl)methanolHCID 12875263—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(Dimethylamino)methyl-3-methylthiopheneHCID 1008066875%

Reaktionsschritte

In 200 ml of methylene chloride were dissolved 20.8 g of 3-methyl-2-thenyl alcohol and 27.1 ml of triethylamine, and 12.9 ml of thionyl chloride was added thereto dropwise at -15° C. to -10° C. over a period of 30 minutes, after which the resulting solution was further subjected to reaction at the same temperature for 30 minutes. The reaction mixture was poured into ice water, and the organic layer was separated and then dried over anhydrous magnesium sulfate. Subsequently, the dried organic layer was added dropwise with ice-cooling to a solution of 95 g of dimethylamine in 550 ml of ethanol, and the resulting mixture was allowed to stand overnight at room temperature. The solvent was removed by distillation under reduced pressure, after which 100 ml of water was added to the residue, and the resulting mixture was adjusted to pH 10 with potassium carbonate, and then extracted with 200 ml of ethyl acetate. The extract was washed with 50 ml of a saturated aqueous sodium chloride solution and dried over anhydrous potassium carbonate, after which the solvent was removed by distillation under reduced pressure, and the oily substance thus obtained was distilled under reduced pressure to obtain 19.0 g (yield 75%) of 2-(dimethylamino)methyl-3-methylthiophene having a boiling point of 85°-86° C./14 mmHg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05120746
Quelldatensatzuspto-grants-1992_06
ORD IDord-b916c9ed0a8f47f9816ec22076886cf8
Quellennotizuspto-grants-1992_06