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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 896997생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1,4-Tetrahydrothiazine-3-oneHCID 88402—
반응물Benzene, 1,2-dichloro-4-iodo-HCID 88591—
촉매copper(I) bromideHCID 24593—
용매DimethylformamideHCID 6228—
생성물4-(3,4-Dichlorophenyl)thiomorpholin-3-oneHCID 988166881%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06921760B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-c065c2a275c2427b84c37e7e45c245e9
출처 메모uspto-grants-2005_07