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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1368364생성일: 2026년 10월 27일

Pentafluoropropionic acid → (2-Pentafluoroethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diaza-cyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1368364

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참여 물질

역할이름HCID투입량
반응물Pentafluoropropionic acidHCID 62356—
반응물[(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochlorideHCID 86586513—
용매DichloromethaneHCID 6344—
생성물(2-Pentafluoroethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diaza-cyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonateHCID 22341386—

반응 단계

A solution of 1.0 g (2.4 mmole) of [(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochloride in 30 mL of pentafluoropropionic acid was refluxed under nitrogen for 6 hours. The mixture was diluted to 400 mL with methylene chloride, washed with 400 mL of water and with 400 mL of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to a crude foam in vacuum. The crude product was column chromatographed on silica gel with 1% methanol in chloroform and the product fractions combined and concentrated in vacuum to give 0.90 g of the (R)-enantiomer of the title compound as a yellow oil. 1H-NMR (CDCl3): doublet 7.75 δ(2H); doublet 7.3 δ(2H); doublet 7.15 δ(1H); doublet 6.9 δ(1H); multiplet 4.5 δ(1h); doublet of doublets 4.25 δ(1H); multiplet 4.2 δ(2H); doublet of doublets 4.1 δ(1H); singlet 2.4 δ(3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06573283B2
출처 데이터셋uspto-grants-2003_06
ORD IDord-115fbe544f9945749dd974e2db9e3848
출처 메모uspto-grants-2003_06