Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminum hydride toluene | HCID 67340441 | — |
| Reactant | HCID 178475130 | HCID 178475130 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178465549 | HCID 178465549 | 66.9% |
Reaction Steps
1-Acetoamido-5-mercapto-1H-tetrazole (1.59 g) was dissolved in anhydrous tetrahydrofuran (27 ml), and the mixture was refluxed. 70% Sodium bis(2-methoxyethoxy)aluminum hydride-toluene solution (5 ml) was added dropwise thereto under stirring. After the addition, the mixture was refluxed for 4 hours. The reaction mixture was evaporated under reduced pressure to remove solvent. Ice-water was added to the residue, and the aqueous solution thus obtained was adjusted to pH 3 with 20% sulfuric acid. The mixture was salted out with sodium chloride, and extracted with ethyl acetate. The extracts were washed with a saturated sodium chloride solution, dried and then evaporated to remove solvent. The residue was recrystallized from isopropyl ether-hexane (1:2) to give 0.97 g of 1-ethylamino-5-mercapto-1H-tetrazole as colorless prisms. mp 90°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04576938 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-3d74e9e62cd5472b8a45d336cfe30696 |
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| Source note | uspto-grants-1986_03 |
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