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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 896997Erstellt: 23. Oktober 2026

Sodium hydride → 4-(3,4-Dichlorophenyl)thiomorpholin-3-one

https://huagongshe.com/de/reaction/896997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1,4-Tetrahydrothiazine-3-oneHCID 88402—
EduktBenzene, 1,2-dichloro-4-iodo-HCID 88591—
Katalysatorcopper(I) bromideHCID 24593—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(3,4-Dichlorophenyl)thiomorpholin-3-oneHCID 988166881%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Under a nitrogen atmosphere in a flame-dried flask, sodium hydride (72 mg, 1.79 mmol, 60% oil dispersion) was washed with hexanes and then treated with 6 mL of anhydrous DMF, and cooled to 0° C. Thiomorpholin-3-one (200 mg, 1.71 mmol) was added in one portion with stirring. After gas evolution had stopped (ca. 30 min), 4-iodo-1,2-dichlorobenzene (700 mg. 2.56 mmol) was added, followed after 5 minutes by copper (I) bromide (490 mg, 3.42 mmol). After heating at 75° C. overnight, the mixture was partitioned between ethyl acetate and 1 N lithium chloride, filtered through diatomaceous earth and combined with additional ethyl acetate washes of the diatomaceous earth filter cake. The organic layers were washed with additional IN lithium chloride, brine (saturated sodium chloride) and dried over calcium sulfate (CaSO4). Concentration in vacuo gave 363 mg of light brown oil which was flash chromatographed (30-50% ethyl acetate in hexanes) to give a white solid, 108 mg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06921760B2
Quelldatensatzuspto-grants-2005_07
ORD IDord-c065c2a275c2427b84c37e7e45c245e9
Quellennotizuspto-grants-2005_07