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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372793Generated: November 3, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 19902089, compound

https://huagongshe.com/reaction/2372793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAdamantanoneHCID 64151—
Reactant1-(3-Fluorobenzyl)-1H-imidazoleHCID 19902087—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19902089HCID 19902089—

Reaction Conditions

Temperature-70 °C

Reaction Steps

55 ml (85 mmol) of a 1.55 molar solution of n-butyllithium in hexane were added dropwise to a solution of 7.04 g (40 mmol) of N-(3-fluorobenzyl)-imidazole and 4.65 g (40 mmol) of N,N,N',N'-tetramethylethylenediamine (TMEDA) in 90 ml of absolute tetrahydrofuran (THF) at -70° C. The mixture was stirred for a further 20 minutes at -70° C., and a solution of 6.01 g (40 mmol) of adamantanone in 30 ml of absolute tetrahydrofuran (THF) was then added dropwise at -70° C. in the course of about 15 minutes. Stirring was then continued for 15 minutes at about -70° C., the reaction mixture was allowed to warm up to room temperature in the course of about 2 hours, 200 ml of water were added at about 5°-18° C., while cooling, and the mixtures was extracted with CH2Cl2. The combined CH2Cl2 extracts were dried, filtered, and evaporated down in vacuo. The residue of the extract was dissolved in acetonitrile, after which crystalline 3-fluorophenyl-(2-hydroxy-2-adamantyl)-imidazolylmethane was precipitated in pure form. After the crystalline product had been filtered off under suction and washed thoroughly with acetonitrile, 8.70 g of pure product of melting point 191° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100890
Source datasetuspto-grants-1992_03
ORD IDord-19f36f7cbb154d0a937c2d44cfa9f03e
Source noteuspto-grants-1992_03