HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N'-t-butyl-N-pyrenonecarbonyl-N'-(3-toluoyl)hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | Pyrenonecarbonyl chloride | HCID 131717420 | — |
| Solvent | Hydroxide | HCID 961 | — |
| Product | N'-t-butyl-N-pyrenonecarbonyl-N'-(3-toluoyl)hydrazine | HCID 131717419 | — |
Reaction Steps
To a stirred suspension of t-butyl hydrazine hydrochloride (0.02 mol) in toluene (20 ml) and aqueous hydroxide (5 ml of 50% solution) at room temperature was added pyrenonecarbonyl chloride (0.01 mol). After stirring the reaction mixture for 20 minutes, ether and hexane were added and the solid product was filtered and washed with water. The solid product (0.5 g) was stirred in toluene (10 ml) and aqueous sodium hydroxide and m-toluoyl chloride (0.8 g) was added dropwise. After stirring for 5 hours, hexane and ether were added and the solid product filtered and air dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424333 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-4ace12a6e29447b3bbd6b021605bd28a |
| Source note | uspto-grants-1995_06 |