HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568725Generated: October 26, 2026
Benzene → N-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidine
https://huagongshe.com/reaction/568725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid | HCID 14210610 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidine | HCID 86742025 | — |
Reaction Steps
To a solution composed of 8.82 g (31.7 mmol) of (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid, 5.66 g of thionyl chloride and 20 ml of benzene was added 2 drops of N,N-dimethylformamide, and the mixture was refluxed for 2 hours. Low-boiling substances were distilled off from the reaction mixture under reduced pressure. The residue was dissolved in 20 ml of dioxane and the solution was added dropwise to a solution composed of 65 millimoles of guanidine, 7.5 ml of ethanol and 25 ml of dioxane at room temperature. Thereafter, the resultant mixture was stirred at room temperature for 1 hour and so obtained reaction mixture was poured into water and extracted with diethyl ether. The ether extract was washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. Low-boiling substances were distilled off under reduced pressure. The residue was purified by silica gel column chromatography and recrystallized from methylene chloride/diethyl ether/n-hexane to give 5.1 g of N-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidine [Compound (1)], which shows the following physical characteristics.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04728650 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-3a7d57c7cac949ea90a3950c4d873126 |
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| Source note | uspto-grants-1988_03 |
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