HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Allylbenzoylhydrazine → S-ethyl S-hexyl O-{3-[2-(3-allylbenzoylhydrazono)ethyl]phenyl} dithiophosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Allylbenzoylhydrazine | HCID 20555786 | — |
| Reactant | S-ethyl S-hexyl O-(3-formylmethylphenyl) dithiophosphate | HCID 86738192 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-ethyl S-hexyl O-{3-[2-(3-allylbenzoylhydrazono)ethyl]phenyl} dithiophosphate | HCID 86738194 | — |
Reaction Steps
A solution of S-ethyl S-hexyl O-(3-Formylmethylphenyl) dithiophosphate (0.02 mole) in methanol (50 ml) and 3-allylbenzoylhydrazine (0.02 mole) are charged into a glass reaction vessel and the mixture is stirred at room temperature for a period of about 12 hours. After this time the reaction mixture is stripped of methanol under vacuum and the residue is dissolved in methylene chloride (100 ml) and the resulting solution is washed with water (75 ml), with aqueous sodium hydroxide (75 ml; 0.1 N) and again with water (75 ml). The washed solution is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent to yield the desired product S-ethyl S-hexyl O-{3-[2-(3-allylbenzoylhydrazono)ethyl]phenyl} dithiophosphate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309422 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-06a8d1e1afd74dae9c3b65a590ab5b7c |
| Source note | uspto-grants-1982_01 |