Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Ethyl-2-oxazoline | HCID 66412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178437959 | HCID 178437959 | — |
Reaction Steps
In a nitrogen flushed flask were mixed 2-ethyl-2-oxazoline (99 g, 1 mole) and anhydrous hydrazine (32 g, 1 mole) in 150 ml of tetrahydrofuran. The mixture was heated 2 hours at 60° C. to obtain a yellow solution. The solvent was stripped to give a pale yellow oil. On standing, white crystals formed. They were recrystallized from 2-propanol to give 3,6-diethyl-1,2-dihydro-1,2,4,5-tetrazine as identified by mass spectroscopy, 13C NMR, and infrared analyses, mp 118.5°-119.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04389327 |
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| Source dataset | uspto-grants-1983_06 |
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| ORD ID | ord-378e644ad6f44dfb8fcb5f177ee2aa5e |
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| Source note | uspto-grants-1983_06 |
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