HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13376456, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Fluoroacetyl chloride | HCID 9663 | — |
| Reactant | HCID 13376448 | HCID 13376448 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13376456 | HCID 13376456 | 91.2% |
Reaction Steps
3.3 g of N-(2-amino-5-nitrobenzoyl)-2-methyl-4-chloroaniline and 1.6 g of pyridine are dissolved in 60 ml of tetrahydrofuran, and 1.93 g of fluoroacetyl chloride are added dropwise thereto under ice-cooling and stirring. The mixture is stirred for 30 minutes under ice-cooling and further stirred at room temperature for 2 hours. The mixture is concentrated under reduced pressure to remove tetrahydrofuran. Water is added to the residue and crystalline precipitates are collected therefrom. The crystals are recrystallized from a mixture of dimethylformamide and ethanol (1:3). 3.6 g of N-(2-fluoroacetamido-5-nitrobenzoyl)-2-methyl-4-chloroaniline are obtained as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04714702 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-40ece020593443a89f1225aae194f604 |
| Source note | uspto-grants-1987_12 |