HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzenamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | 4-chloro-N,N-bis(4-fluorophenyl)butanamide | HCID 15087788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzenamine | HCID 14722551 | 91.5% |
Reaction Steps
To a stirred and cooled (0° C.) solution of 48 parts of 4-chloro-N,N-bis(4-fluorophenyl)butanamide in 108 parts of tetrahydrofuran were added 240 parts of a solution of borane, compound with thiobismethane, in tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was decomposed with 160 parts of methanol. After evaporation, The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and petroleum ether (20:80 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 32.5 parts (91.5%) of N-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzeneamine as a residue (int. 70).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026853 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-d2e5fc034c1d4792961653f083215c7d |
| Source note | uspto-grants-1991_06 |