HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178449878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | HCID 54490127 | HCID 54490127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178449878 | HCID 178449878 | — |
| Product | HCID 178449879 | HCID 178449879 | — |
Reaction Steps
A mixture of 2-(3-bromobenzoyl)-3-hydroxypyridine 1-oxide (2.13 g), t-butylhydrazine hydrochloride (3.03 g), triethylamine (3.5 mL) and ethanol (50 mL) was refluxed for 2 hours. The reaction mixture was then poured into a saturated aqueous saline solution, and subjected to extraction with ethyl acetate. The extract was washed with a saturated aqueous saline solution, and dried (sodium sulfate), followed by evaporating the solvent under reduced pressure. The residue was purified by means of a silica gel column (ethyl acetate--hexane) to afford (E)-2-(3-bromo-t-butylhydrazonobenzyl)-3-hydroxypyridine 1-oxide (0.68 g) and (Z)-2-(3-bromo-α-t-butylhydrazonobenzyl)-3-hydroxypyridine 1-oxide (0.79 g) (compounds 29 and 28).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891895 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-6772afe0daa7403abc75ab2e401c2617 |
| Source note | uspto-grants-1999_04 |