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HRID 239235생성일: 2026년 10월 23일

Lawesson's reagent → Oxane-4-carbothioamide

https://huagongshe.com/ko/reaction/239235

반응식

참여 물질

역할이름HCID투입량
반응물Lawesson's reagentHCID 87949—
반응물Sodium BicarbonateHCID 516892—
반응물Oxane-4-carboxamideHCID 13197203—
용매TetrahydrofuranHCID 8028—
생성물Oxane-4-carbothioamideHCID 1319720487.5%

반응 단계

A solution of tetrahydro-2H-pyran-4-carboxamide (9.47 g, 73.3 mmol) and Lawesson's reagent (14.83 g, 36.7 mmol) in THF (98 mL) was heated to reflux for 6 h. The reaction was cooled to rt, poured into saturated aqueous NaHCO3 (200 mL) and extracted with diethyl ether (4×100 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated. The residual solid was triturated with 1:1 EtOAc:hexanes (100 mL) and filtered to collect the solid. The filtrate was concentrated and re-subjected to trituration and filtration using the same conditions. The combined solids were dried under vacuum to afford tetrahydro-2H-pyran-4-carbothioamide (4.91 g, 32.1 mmol, 43.8% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.49 (br. s., 1H), 6.84 (br. s., 1H), 3.94-4.32 (m, 2H), 3.31-3.62 (m, 2H), 2.52-3.03 (m, 1H), 1.81-1.93 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642759B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7da2d16f7e3c417fa2892031a82a7d54
출처 메모uspto-grants-2014_02