HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N'-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbohydrazonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbohydrazonoyl chloride | HCID 131733232 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N'-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbohydrazonamide | HCID 117965458 | — |
Reaction Conditions
| Temperature | 2.5 °C |
|---|
Reaction Steps
To a cold solution of N-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbohydrazonoyl chloride (0.070 g, 0.267 mmol) in dry THF was added aq. ammonia. The reaction mass was stirred at 0-5° C. for 2-3 h. The reaction mass was quenched in water, neutralized with dilute acetic acid and extracted with DCM. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 0.040 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 6.29 (br s, 2H), 6.80 (d, J=8.4 Hz, 2H), 7.24 (d, J=9.3 Hz, 2H), 7.28-7.50 (m, 3H), 8.33 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09439890B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-e3b3e7e8935b47088e554424e5b52271 |
| Source note | uspto-grants-2016_09 |