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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636423Generated: November 2, 2026

Formaldehyde → 1H-Imidazole-5-methanol, 2-butyl-1-[(2-chlorophenyl)methyl]-

https://huagongshe.com/reaction/1636423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium AcetateHCID 517045—
Reactant1H-Imidazole, 2-butyl-1-[(2-chlorophenyl)methyl]-HCID 10377357—
SolventAcetic AcidHCID 176—
Product1H-Imidazole-5-methanol, 2-butyl-1-[(2-chlorophenyl)methyl]-HCID 1001641841.1%

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 resiue was stirred with 500 mL of 20% sodium hydroxide solution for 4 hours, diluted with water and extracted with methylene chlordie. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034114
Source datasetuspto-grants-2000_03
ORD IDord-2d1689e83f2c47da8fcf45774eef91fd
Source noteuspto-grants-2000_03