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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291045Generated: October 27, 2026

Ammonium Chloride → [4-(2-Methylimidazol-1-yl)phenyl]methanol

https://huagongshe.com/reaction/1291045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Methyl-1H-imidazol-1-yl)benzaldehydeHCID 3159662—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product[4-(2-Methylimidazol-1-yl)phenyl]methanolHCID 1173561750.5%

Reaction Steps

To a stirred solution of the crude 4-(2-methylimidazol-1-yl)benzaldehyde (1.0 g) in methanol(15 ml) cooled to 0° C. was added NaBH4 (0.2 g, 5.2 mmol) in portions over 15 min and the whole stirred for 1 h. A saturated aqueous NH4Cl solution (50 ml) was added to the reaction mixture and the whole extracted with ethyl acetate (100 ml×2). The organic layer was washed with water (100 ml), brine (50 ml), dried over MgSO4, and solvent removed under reduced pressure. The crude product was washed with an Et2O/ethyl acetate mixture (3:1, 15 ml) to give the title compound (0.51 g, 50 %) as a white powder. 1H NMR (CDCl3) δ: 7.5 (d, 2H, J=8 Hz), 7.28 (d, 2H, J=8 Hz), 7.01 (d, 1H, J=1 Hz), 6.99 (d, 1H, J=1 Hz), 4.78 (s, 2H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753682
Source datasetuspto-grants-1998_05
ORD IDord-bc71e60e4a684e24aa7197a8d701537d
Source noteuspto-grants-1998_05