HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21662Generated: October 26, 2026
Triethylamine → N'-t-butyl-N-benzoyl-N'-methylpyridinylhydrazine
https://huagongshe.com/reaction/21662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Picolyl chloride | HCID 23393 | — |
| Reactant | N'-tert-butylbenzohydrazide | HCID 299436 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N'-t-butyl-N-benzoyl-N'-methylpyridinylhydrazine | HCID 19368177 | 20% |
Reaction Steps
N'-t-butyl-N-benzoyl hydrazine (1.2 g), 2-chloromethyl pyridine (1.0 g) and triethylamine (2 equivalents) were stirred in dimethyl sulfoxide (15 ml) at room temperature for 2 hours. The reaction mixture was then warmed to 50° C. for 2 hours. The mixture was diluted with ether and washed with water. The organic layer was dried over magnesium sulfate, filtered and rotavapped to afford a yellow oil. The oil was chromatographed on silica gel (G:70-230 mesh) using a methylene chloride-ether mixture (1:1) as eluant to afford the purified product as a yellow gum in approximately 20% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05424333 |
|---|
| Source dataset | uspto-grants-1995_06 |
|---|
| ORD ID | ord-682d8d43834e4d31a8179b4d5b542b64 |
|---|
| Source note | uspto-grants-1995_06 |
|---|