HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pivaloyl chloride → Pivalic acid 2-(2-bromo-4-nitrophenyl)hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-4-nitro-phenyl-hydrazine | HCID 3780065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Pivalic acid 2-(2-bromo-4-nitrophenyl)hydrazide | HCID 53671610 | 60.7% |
Reaction Steps
To a stirred and chilled (0°) solution containing 200 g (0.86 mol) of 2-bromo-4-nitrophenylhydrazine (m.p. 143°-145°) and 116.8 g (0.9 mol) of ethyldiisopropylamine in 1000 ml of tetrahydrofuran was added dropwise 108.5 g (0.9 mol) of pivaloyl chloride. The reaction mixture was stirred at ambient temperature for 1 hour and then concentrated to dryness under reduced pressure. The residue was treated with water, filtered and recrystallized from ethanol to give 165 g (52%) of product as a light yellow solid; m.p. 145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174958 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-190279ac6ac94ac49644cabe172141dd |
| Source note | uspto-grants-1979_11 |