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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606590Erstellt: 24. Oktober 2026

Morpholine → (5-Bromo-4-methylthiophen-2-yl)(morpholin-4-yl)methanone

https://huagongshe.com/de/reaction/606590

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
EduktSodium HydroxideHCID 14798—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktMethyl 5-bromo-4-methylthiophene-2-carboxylateHCID 2795489—
Edukt5-Bromo-4-methylthiophene-2-carboxylic acidHCID 21899459—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(5-Bromo-4-methylthiophen-2-yl)(morpholin-4-yl)methanoneHCID 67047076—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

5-Bromo-4-methyl-thiophene-2-carboxylic acid methyl ester (8.51 mmol) was dissolved in EtOH (100 ml) and NaOH (42.5 mmol) added, as a 1M solution in water. Reaction was heated to 80° C. for 2 h, after which time all starting material had been consumed. Reaction was then concentrated in vacuo and the residue taken up in DCM and shaken with 1M HCl. The resulting biphasic mixture was then filtered and the filtrant washed with hexane and dried under vacuum. This gave 5-Bromo-4-methyl-thiophene-2-carboxylic acid as off white solid: m/z in MS AP−=219, 221 [M−H]−, 6.79 mmol, 80%. 5-Bromo-4-methyl-thiophene-2-carboxylic acid (6.79 mmol) was taken up in 30 ml DMF and morpholine (7.47 mmol), WSC.HCl (7.47 mmol) and HOBt (7.47 mmol) were added. Reaction was stirred at room temperature for 17 h and then diluted with EtOAc, washed with 1M HCl and brine, dried over Na2SO4 and concentrated in vacuo. Flash chromatography of the residue (silica, 33-50% EtOAc in hexane) gave (5-Bromo-4-methyl-thiophen-2-yl)-morpholin-4-yl-methanone as a pale golden oil: m/z in MS ES+=290, 292 [M+H]+, 4.67 mmol, 69%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915300B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-d96bba80fb7c4d03932edfc7208efdb1
Quellennotizuspto-grants-2011_03