HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzaldehyde → N-[(4-Fluorophenyl)methylene]-1H-1,2,4-triazol-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 1H-1,2,4-triazol-1-amine | HCID 11708047 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[(4-Fluorophenyl)methylene]-1H-1,2,4-triazol-1-amine | HCID 54271016 | 68.3% |
Reaction Steps
A solution of 42.3 g (0.377 mol) of 75% pure 1-amino-1H-1,2,4-triazole, 40.0 mL (0.372 mol) of 4-fluorobenzaldehyde and 2.0 g of p-toluenesulfonic acid in 600 mL of tetrahydrofuran was stirred at room temperature for 21/2 days. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous Na2CO3, water and brine and dried (MgSO4). Removal of solvent gave a white solid which was recrystallized from n-butylchloride to afford 48.3 g (67%) of desired product as white needles; mp 118°-120° C. Concentration of the filtrate and recrystallization of the residue afforded 12.8 g (18%) more of product; mp 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041458 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-11be9ab357cd4cbd8e6f3ccf371198fa |
| Source note | uspto-grants-1991_08 |