HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267325Generated: November 1, 2026
4-Chlorobenzaldehyde → HCID 178506597, compound
https://huagongshe.com/reaction/267325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | HCID 178506596 | HCID 178506596 | — |
| Reactant | HCID 178513178 | HCID 178513178 | — |
| Product | HCID 178506597 | HCID 178506597 | — |
Reaction Steps
In a similar manner the reaction of 1-amino-3-(4-bromobenzylideneamino)guanidine methosulfate with 4-chlorobenzaldehyde gives the methosulfate salt of the subject compound. The reaction of 1-amino-3-(4-cyanobenzylideneamino)guanidine hydroiodide with 4-chlorobenzaldehyde gives 1-(4-chlorobenzylideneamino)-3-(4-cyanobenzylideneamino)guanidine hydroiodide; the reaction of 1-amino-3-(4-chlorobenzylideneamino)guanidine hydrochloride with 4-cyanobenzaldehyde affords the corresponding hydrochloride salt which melts at 297°-298°C. The reaction of 1-amino-3-(3,4-dichlorobenzylideneamino)guanidine hydrobromide and 4-chlorobenzaldehyde gives 1-94-chlorobenzylideneamino)-3-(3,4-dichlorobenzylidenamino)guanidine hydrobromide; the reaction of 1-amino-3-(4-chlorobenzylideneamino)guanidine hydrochloride with 3,4-dichlorobenzaldehyde gives the corresponding hydrochloride salt which melts at 288°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03941825 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-ba51ea80c5344e45b5c1dc2d35c71b16 |
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| Source note | uspto-grants-1976_03 |
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