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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194369Generated: November 1, 2026

Water → HCID 14520333, compound

https://huagongshe.com/reaction/1194369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
ReactantHCID 178418682HCID 178418682—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14520333HCID 1452033358%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 0.22 mole of n-butyl magnesium bromide in 75 ml of tetrahydrofuran is slowly added, under an atmosphere of argon, to 67.6 g (0.2 mole) of 1-triphenylmethyl-1H-imidazole-4-carboxaldehyde (obtained as described in 1.b. above) in 500 ml of tetrahydrofuran. The temperature of the mixture is maintained at about 20° C. by cooling on an ice-bath. When the addition is complete, stirring is maintained for 30 minutes at ambient temperature and then 11 g of ammonium chloride and 100 ml of water are successively added. The mixture is extracted with dichloromethane. The organic phases are dried over anhydrous sodium sulfate, then evaporated under reduced pressure. The residue is recrystallized from a 2:1 v/v ethyl acetate-diethyl ether mixture. 45.8 g of alpha-n-butyl-1-triphenylmethyl-1H-imidazole-4-methanol are obtained. Yield: 58% of theory; M.P.: 119°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814343
Source datasetuspto-grants-1989_03
ORD IDord-7106cfe16f6c4a27b6f56ec0567e358e
Source noteuspto-grants-1989_03