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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392676생성일: 2026년 10월 24일

Trifluoroacetic acid → (2-Trifluoromethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diazacyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/ko/reaction/392676

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물[(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochlorideHCID 86586513—
용매DichloromethaneHCID 6344—
생성물(2-Trifluoromethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diazacyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonateHCID 22341388—

반응 단계

A solution of 3.1 g (7.3 mmole) of [(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochloride in 50 mL of trifluoroacetic 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 3.3 g of the (R)-enantiomer of the title compound as a white solid (m.p. 114-116° C.), which retains one equivalent of chloroform.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06803368B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-4879152fb38b4a70a3235e3da4bb9941
출처 메모uspto-grants-2004_10