HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419794Generated: October 31, 2026
Hydrochloric Acid → HCID 178479328, compound
https://huagongshe.com/reaction/2419794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Trifluoromethyl)benzylamine | HCID 75962 | — |
| Reactant | Methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodide | HCID 178504060 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178479328 | HCID 178479328 | — |
Reaction Steps
A solution of 4.88 g. of methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodide (U.S. Pat. No. 3,657,337) and 4.37 g. of m-(trifluoromethyl)benzylamine [F. N. Freidfelder and Y. H. Ng, J. Pharm. Sci., 54, 1204 (1965)] in 270 ml. of absolute ethanol is heated at reflux for 18 hours. The solution is cooled, made basic with 2N NaOH and the solvent is removed under reduced pressure. The yellow residue is triturated with dichloromethane and the triturate is evaporated under reduced pressure to give a yellow oil. A diethyl ether solution of this oil is treated with ethanolic hydrogen chloride. Filtration gives colorless crystals which are recrystallized from ethanol-diethyl ether, giving the desired product as colorless crystals, m.p. 165°-167° 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-e8f8bc08de034ee8b2fc421ae65b0956 |
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| Source note | uspto-grants-1978_08 |
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