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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 974550생성일: 2026년 10월 24일

Methyl isothiocyanate → N-Methyl-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide

https://huagongshe.com/ko/reaction/974550

반응식

참여 물질

역할이름HCID투입량
반응물Methyl isothiocyanateHCID 11167—
반응물3-[3-(Trifluoromethyl)phenoxy]azetidineHCID 11138538—
반응물1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 11728694—
용매DichloromethaneHCID 6344—
생성물N-Methyl-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamideHCID 15053382—

반응 단계

Crude 3-[3-(trifluoromethyl)phenoxy]azetidine from catalytic debenzylation of 26.0 g (0.078 mole) of 1-benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidine was dissolved in 100 ml of methylene chloride and treated dropwise under a nitrogen atmosphere with a solution of 5.0 g (0.0678 mole) of methylisothiocyanate in 15 ml of methylene chloride. The reaction mixture was stirred for 16 hr at ambient temperature and let stand over the weekend. The solution was filtered through a celite filter pad to remove a fine crystalline precipitate and the filtrate was evaporated under reduced pressure. The residual oil was crystallized from isopropyl ether to give 12.6 g of product, m.p. 78°-86° C. A 5.0 g sample was recrystallized from isopropyl ether (charcoal) to give 3.2 g, m.p. 89°-93° C., which was shown by TLC on silica gel (10% methanol-toluene) to be contaminated by a lower Rf material. The filtrate was evaporated under reduced pressure, combined with the 3.2 g of solid and dissolved in 100 ml of methylene chloride. The solution was stirred with 25 g of silica gel for 0.5 hr and filtered through a sintered glass filter. The silica gel was washed with a small volume of methylene chloride and the filtrate evaporated under reduced pressure. The residual solid was recrystallized from isopropyl ether to give 1.3 g of pure product, m.p. 96°-98° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05068231
출처 데이터셋uspto-grants-1991_11
ORD IDord-c835af300e14466092cf19bfda3dec3c
출처 메모uspto-grants-1991_11