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HRID 2081389作成日:2026年10月27日

2,6-Xylyl isothiocyanate → N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide

https://huagongshe.com/reaction/2081389

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Xylyl isothiocyanateHCID 87976—
反応物3-[3-(Trifluoromethyl)phenoxy]azetidineHCID 11138538—
反応物1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 11728694—
溶媒DichloromethaneHCID 6344—
生成物N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamideHCID 15053383—

反応手順

Crude 3-[3-(trifluoromethyl)phenoxy]azetidine from catalytic debenzylation of 30.0 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 12.7 g (0.078 mole) of 2,6-dimethylphenylisothiocyanate in 25 ml of methylene chloride. The product began to precipitate during the addition and an additional 50 ml of methylene chloride was added to facilitate stirring. After stirring overnight at ambient temperature, the product was collected by filtration (13.5 g, m.p. 196°-199° C.) A 6.0 g sample was recrystallized from isopropanol to give 5.3 g of product, m.p. 197°-199° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05183902
出典データセットuspto-grants-1993_02
ORD IDord-1b170b8704634204b155fd8f7f8acbb2
出典メモuspto-grants-1993_02