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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536969생성일: 2026년 10월 26일

Sodium hydride → 4-(4-Nitro-phenyl)-1,1-dioxo-hexahydro-1lambda6-thiopyran-4-carbonitrile

https://huagongshe.com/reaction/536969

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물p-NitrophenylacetonitrileHCID 68386—
반응물1-Bromo-2-(2-bromoethanesulfonyl)ethaneHCID 139052—
용매Dimethyl SulfoxideHCID 679—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Nitro-phenyl)-1,1-dioxo-hexahydro-1lambda6-thiopyran-4-carbonitrileHCID 5899493298.3%

반응 단계

A slurry of NaH (71.4 mg, 1.79 mmol, 60% dispersion) in DMSO (3 mL) and THF (1 mL) was treated with solid (4-nitro-phenyl)-acetonitrile (121 mg, 0.744 mmol) and stirred at RT for 3 min. A solution of 1-bromo-2-(2-bromoethanesulfonyl)-ethane (250 mg, 0.893 mmol) in THF (3 mL) was added, and the mixture was heated to 70° C. for 1.5 h. The mixture was partitioned between EtOAc (100 mL) and water (75 mL), and brine (25 mL) was added. The aqueous layer was extracted with EtOAc (1×50 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo. Silica gel chromatography of the residue on a 20-g Isolute SPE column with 10-50% EtOAc-hexane afforded the title compound (205 mg, 98%) as a white solid. 1H-NMR (CDCl3; 400 MHz): δ 8.33 (d, 2H, J=8.8 Hz), 7.75 (d, 2H, J=8.8 Hz), 3.64-3.52 (m, 2H), 3.29-3.19 (m, 2H), 2.88-2.76 (m, 2H), 2.54-2.44 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859602B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-e4f0fccac76b4ab58a7b51bfd973badd
출처 메모uspto-grants-2014_10