Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,6-Xylyl isothiocyanate → N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
| 반응물 | 3-[3-(Trifluoromethyl)phenoxy]azetidine | HCID 11138538 | — |
| 반응물 | 1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidine | HCID 11728694 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide | HCID 15053383 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05068231 |
| 출처 데이터셋 | uspto-grants-1991_11 |
| ORD ID | ord-ae1dadd083204312b259b840f3cd45b5 |
| 출처 메모 | uspto-grants-1991_11 |