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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231282Generated: October 31, 2026

Formaldehyde → 1-Methyl-3-hydroxymethyl-4-imidazolin-2-one

https://huagongshe.com/reaction/231282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant1-methyl-2,3-dihydro-1H-imidazol-2-oneHCID 566589—
SolventAcetoneHCID 180—
Product1-Methyl-3-hydroxymethyl-4-imidazolin-2-oneHCID 14245714—

Reaction Steps

A mixture of 1-methyl-4-imidazolin-2-one (4 gms, 0.04 mol), 20 ml of formaldehyde (37% aqueous solution), sodium hydroxide (100 mg), and 20 ml of methanol was stirred at room temperature for 20 hours. After removing the solvent using a rotovap at reduced pressure, a liquid residue was obtained and filtered through a column of silica gel using chloroform as the eluent. The residue solidified after left standing overnight and was dissolved in water and then extracted with chloroform. The aqueous phase was concentrated and chromatographed through a column of silica gel G 60. Removal of the solvent afforded a solid which upon addition of acetone became white suspension. The solid was washed twice with acetone and air-dried (1.0 gm, 22%) and sublimed at reduced pressure, m.p. 101.5°-103.5° C. Found: C, 46.70; H, 6.18: N, 21.80. Calc. for C5H8N2O2 : C, 46.87; H, 6.29; N, 21.86%. 1H n.m.r.(CDCl3 ): δ3.15(3H, s, CH3N--); 5.02(2H, s, broad, N-CH2OH); 5.8(1H, s, broad, OH); 6.1 (1H, d, J=3 Hz, HC-CH); 6.3(1H, d, J=3 Hz, HC=CH). νmax (KBr): 3220(OH, broad); 3120, 3100(HC=CH); 1655 cm-1 (C=O). m/e 128, C5H8N2O2 requires 128.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845233
Source datasetuspto-grants-1989_07
ORD IDord-3e90c0d9255d4ad5bfbc90dd2f022d60
Source noteuspto-grants-1989_07