HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703633Generated: October 30, 2026
Butanedione → 1H-Imidazole-4-methanol, 5-methyl-2-phenyl-
https://huagongshe.com/reaction/1703633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butanedione | HCID 650 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzamidine, hydrochloride | HCID 80289 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-Imidazole-4-methanol, 5-methyl-2-phenyl- | HCID 83658 | — |
Reaction Steps
A 100 gm. portion of benzamidine hydrochloride is dissolved in a minimum of water (350 ml.) at room temperature. A 67 gm. portion of freshly distilled 2,3-butanedione is added giving a yellow solution. Adjusting the pH to 6-7 with 2N NaOH gives a solid which is allowed to stand at 0° C. for 2 hours, collected, pressed dry and then washed with 100 ml. of acetone. This material is heated with stirring on a steam bath with 855 ml. of concentrated HCl and 2437 ml. of water for 4 hours giving a solution. Cooling to room temperature overnight and then to 0° C. produces a solid which is collected and air dried. This solid is dissolved in 350 ml. of ethanol, filtered and cooled producing a gel, which is taken up in 250 ml. of 50°-60° C. water, adjusted to pH 5.5 with concentrated NaOH and then to pH 7-8 with solid KHCO3. The mixture is cooled to 0° C. and the product is collected, washed with water, and air dried. This product is recrystallized from 1 liter of methanol giving the final product, m.p. 197°-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04124766 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-8b01d0842485441f88b4e57fd12a70a1 |
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| Source note | uspto-grants-1978_11 |
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