HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85239Generated: October 27, 2026
Ammonium Acetate → HCID 86667539, compound
https://huagongshe.com/reaction/85239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-[3-Cyano-4,5,5-trimethylfuran-2(5H)-ylidene]malononitrile | HCID 9990345 | — |
| Reactant | 5-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]thiophene-2-carboaldehyde | HCID 86667538 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86667539 | HCID 86667539 | 75.1% |
Reaction Steps
In 10 ml of ethanol and 3 ml of tetrahydrofuran were dissolved 300 mg (0.81 mmol) of 5-[2-(4-dibutylamino-2-methoxyphenyl)vinyl]thiophene-2-carboaldehyde and 177 mg (0.89 mmol) of 2-(3-cyano-4,5,5-trimethyl-2(5H)-furanylidene)propanedinitrile. To this mixture was added 63 mg of ammonium acetate, and the mixture was stirred at room temperature for 24 hours and further at 50° C. for 2.5 hours. The solvent was evaporated off and the residue was washed with ethanol to give 335 mg of a brown powdered crystal (yield: 75.1%; mp: 191-192° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846955B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2bf69ea862a6454f898767a1d5b5154e |
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| Source note | uspto-grants-2014_09 |
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