HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36616Generated: October 25, 2026
Formaldehyde → 2,2-Dimethyl-6-(1H-imidazol-1-YL)benzopyran
https://huagongshe.com/reaction/36616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Glyoxal | HCID 7860 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2,2-Dimethyl-2H-chromen-6-amine | HCID 10080881 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2-Dimethyl-6-(1H-imidazol-1-YL)benzopyran | HCID 19937600 | — |
Reaction Steps
To a stirred solution of 20 g (0.11 mol) of 6-amino-2,2-dimethylbenzopyran and 70 g (0.91 mol) of ammonium acetate in 190 mL of acetic acid and 770 mL of MeOH at 65° C. is added dropwise over 0.5 h, a mixture of 11.1 g (0.14 mol) of formaldehyde and 20g (0.14 mol) of glyoxal. The mixture is stirred for 1 hour at 65° C., then poured onto 800 g of ice. The pH of the solution is adjusted to 10 by the addition of concentrated ammonium hydroxide. The mixture is extracted with dichloromethane (3×200 mL) and the combined organic extracts are dried with sodium sulfate, filtered and evaporated under reduced pressure. The resulting oil is subjected to chromatography on silica gel utilizing 3% methanol in dichloromethane as eluent. The eluates are analyzed utilizing thin layer chromatography and appropriate fractions are combined and evaporated to produce the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05416097 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-90b75e363fa247b8ab5b0c4afb592cd3 |
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| Source note | uspto-grants-1995_05 |
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