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2,6-Xylyl isothiocyanate → N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
| 反応物 | 3-[3-(Trifluoromethyl)phenoxy]azetidine | HCID 11138538 | — |
| 反応物 | 1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidine | HCID 11728694 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide | HCID 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 addition 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05068231 |
| 出典データセット | uspto-grants-1991_11 |
| ORD ID | ord-ae1dadd083204312b259b840f3cd45b5 |
| 出典メモ | uspto-grants-1991_11 |