Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodide | HCID 178504060 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178506600 | HCID 178506600 | — |
Reaction Steps
A solution of 5.85 g. of methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodide (U.S. Pat. No. 3,657,337) and 3.75 g. of p-fluorobenzylamine in 25 ml. of absolute ethanol is heated under reflux for 24 hours and then evaporated under reduced pressure, giving a mixture of gum and crystals. This mixture is dissolved in 50 ml. of absolute ethanol and diluted with 175 ml. of diethyl ether. The colorless plates which form are removed by filtration and discarded. The filtrate is diluted with petroleum ether (b.p. 30°-60° C), causing colorless needles to separate. These needles are removed by filtration and recrystallized from a mixture of ethanol-diethyl ether-petroleum ether (b.p. 30°-60° C), giving the desired product as colorless crystals, m.p. 162.5°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04107326 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-c453b6f518ae4a0fbf3e67178a8ebdfb |
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| Source note | uspto-grants-1978_08 |
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