Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 70157188 | HCID 70157188 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59896634 | HCID 59896634 | 48.8% |
Reaction Steps
To 2.59 g (0.01 mole) of 1-(4-chlorobenzyl)amino-1-methylthio-2-nitroethylene were added 45 ml of EtOH, 10 ml of THF and 1.02 g of 25% aqueous ammonia and the mixture was stirred at an external temperature of 60° C. for 5.5 hours. During this period, 1.02 g each of 25% aqueous ammonia was added after 1, 2 and 3 hours of reaction. The reaction mixture was ice-cooled and stirred, whereupon crystals separated out. The crystals were collected by filtration, washed with EtOH and ether in that order, and dried. The procedure gave 1.11 g of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214152 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-6e865ff668ab4fb29bb15c6a6c457e89 |
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| Source note | uspto-grants-1993_05 |
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