HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 12632313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 19041234 | HCID 19041234 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12632313 | HCID 12632313 | 93.6% |
Reaction Steps
A mixture of 15 g (64 mmol) of ethyl α-(4-methylbenzoyl)isobutyrate, 10 g (93 mmol) of phenyl-hydrazine and 100 ml of toluene was dehydrated under reflux in the presence of p-toluenesulfonic acid monohydrate (catalytic amount) for 18 hours. The reaction solution was washed successively with 1N sodium hydroxide, 1N hydrochloric acid and saturated brine solution, and dried over anhydrous magnesium sulfate. Then the solvent was evaporated under reduced pressure. The obtained crude product was recrystallized from methanol to give 15 g of the object compound as white crystals (yield 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05639776 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-2e9cadc04c5d49d1bbb9e19eb637f841 |
| Source note | uspto-grants-1997_06 |