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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1253327생성일: 2026년 10월 27일

Acetonitrile → 8-(4-(Methylsulfonyl)phenyl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/1253327

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
반응물1-Fluoro-4-(methylsulphonyl)benzeneHCID 67994—
용매WaterHCID 962—
생성물8-(4-(Methylsulfonyl)phenyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 425636077.3%

반응 단계

A mixture of 10 g (0.057 mol) of p-fluorophenyl methyl sulfone, 8.72 g (0.063 mol) of K2CO3, 24.66 g (0.172 mol) of 1,4-dioxa-8-azaspiro[4.5]decane, and 50 ml of acetonitrile is stirred overnight at 90°-100° C. After cooling, the mixture is diluted with water and extracted with methylene chloride. The combined extracts are washed with brine, dried over Na2SO4, and concentrated in vacuo. Trituration with ether affords 13.11 g (77%) of title compound as a white solid: m.p. 192°-194° C.; IR (KBr) 1588, 1369, and 1290 cm-1 ; NMR (CDCl3) δ 7.74 (m, 2H), 6.96 (m, 2H), 4.02 (s, 4H), 3.54 (m, 4H), 3.03 (s, 3H), 1.81 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04748246
출처 데이터셋uspto-grants-1988_05
ORD IDord-b36c1ff0aa1544ee989519f9babb580b
출처 메모uspto-grants-1988_05