HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616103Generated: October 29, 2026
Hydrochloric Acid → HCID 10657374, compound
https://huagongshe.com/reaction/616103
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 10563608 | HCID 10563608 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 10657374 | HCID 10657374 | — |
Reaction Steps
1.2 G. of 2-amino-4-(4-chlorophenoxy)-1-nitrobenzene in 3ml. concentrated hydrochloric acid is treated with a solution of 6 g. stannous chloride in 3 ml. concentrated hydrochloric acid. The mixture is heated briefly (about ten minutes) on a steam bath, then cooled and treated with potassium bicarbonate and chloroform. The chloroform layer is removed from the filtered mixture, dried and evaporated. 1,2-diamino-4-(4-chlorophenoxy)benzene is isolated as a gum. 1G. of 1,2-diamino-4-(4-chlorophenoxy)benzene in 20 ml. acetone is treated overnight at room temperature with 2.5 g. methoxy carbonyl isothiocyanate. The mixture is concentrated under vacuum and the residue triturated with methanol. Recrystallization from methanol gives pure 1,2-bis-(3-methoxycarbonyl-2-thioureido)-4-(4-chlorophenoxy)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04072696 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-6f991493f20e4f3f87e16c7784473abb |
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| Source note | uspto-grants-1978_02 |
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