HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260735Generated: October 26, 2026
Formaldehyde → 1H-Imidazole-5-methanol, 2-butyl-1-[(2-chlorophenyl)methyl]-
https://huagongshe.com/reaction/260735
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1H-Imidazole, 2-butyl-1-[(2-chlorophenyl)methyl]- | HCID 10377357 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1H-Imidazole-5-methanol, 2-butyl-1-[(2-chlorophenyl)methyl]- | HCID 10016418 | 41.1% |
Reaction Steps
A mixture of 2-n-butyl-1-(2-chlorophenyl)methyl-1H-imidazole (95.5 g, 0.384 mol), 37% formaldehyde (500 mL), sodium acetate (80 g) and acetic acid (60 mL) was heated to reflux for 40 hours under argon. The reaction was concentrated in vacuo, and the residue was stirred with 500 mL of 20% sodium hydroxide solution for 4 hours, diluted with water and extracted with methylene chloride. The extract was washed, dried, and concentrated. The crude product (117 g) was flash chromatographed over 600 g of silica gel with a gradient of ethyl acetate to 10% of methanol in ethyl acetate to give 8.3 g of starting material, 24.5 g of a mixture of starting material and product, and 44 g (41%) of 2-n-butyl-1-(2-chlorophenyl)methyl-5-hydroxymethyl-1H-imidazole; mp 86°-88° C. (from ethyl acetate). Further elution provided the bis (4,5-hydroxymethyl) derivative; mp 138°-140° C. (from ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05530017 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-25cb2dd7797b4a8ebc88284fdaa35bc9 |
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| Source note | uspto-grants-1996_06 |
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