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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974555생성일: 2026년 10월 24일

Allyl isocyanate → N-(2-Propenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide

https://huagongshe.com/ko/reaction/974555

반응식

참여 물질

역할이름HCID투입량
반응물Allyl isocyanateHCID 15123—
반응물3-[4-(Trifluoromethyl)phenoxy]azetidineHCID 12812499—
용매Diisopropyl EtherHCID 7914—
생성물N-(2-Propenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamideHCID 15053419—

반응 단계

A solution of 8.7 g (0.04 mole) of crude 3-[4-(trifluoromethyl)phenoxy]azetidine in 75 ml of isopropyl ether was stirred under a blanket of nitrogen while 4.2 g (0.05 mole) of 2-propenyl isocyanate was added dropwise. After stirring for 3 days, no crystalline product precipitated. The reaction mixture was concentrated to a dark reddish oil. TLC (20% ethyl acetate/methylene chloride on silica gel) showed at least 6 spots, all well separated. The residue was dissolved in chloroform, chromatographed on a 350 g silica gel column and eluted with chloroform until the reddish forerun was removed. The column was then eluted with an ethyl acetate/chloroform gradient to 4% ethyl acetate. All the fractions were combined and concentrated to give 4.8 of orange oil, which crystallized on standing. Recrystallization from acetone/cyclohexane gave 3.3 g (27.5%) of being crystals, m.p. 91°-92.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05068231
출처 데이터셋uspto-grants-1991_11
ORD IDord-2d60b1d155fa44878f040481b455c353
출처 메모uspto-grants-1991_11