HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Xylyl isothiocyanate → N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
| Reactant | 3-[3-(Trifluoromethyl)phenoxy]azetidine | HCID 11138538 | — |
| Reactant | 1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidine | HCID 11728694 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,6-Dimethylphenyl)-3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbothioamide | HCID 15053383 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068231 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-ae1dadd083204312b259b840f3cd45b5 |
| Source note | uspto-grants-1991_11 |