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HRID 1032099作成日:2026年10月26日

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

https://huagongshe.com/reaction/1032099

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US04956359
出典データセットuspto-grants-1990_09
ORD IDord-7bbf08df0a04472389d576c1149ade50
出典メモuspto-grants-1990_09