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HRID 896997作成日:2026年10月25日

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

https://huagongshe.com/reaction/896997

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1,4-Tetrahydrothiazine-3-oneHCID 88402—
反応物Benzene, 1,2-dichloro-4-iodo-HCID 88591—
触媒copper(I) bromideHCID 24593—
溶媒DimethylformamideHCID 6228—
生成物4-(3,4-Dichlorophenyl)thiomorpholin-3-oneHCID 988166881%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06921760B2
出典データセットuspto-grants-2005_07
ORD IDord-c065c2a275c2427b84c37e7e45c245e9
出典メモuspto-grants-2005_07