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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493739Generated: October 28, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 67919426, compound

https://huagongshe.com/reaction/1493739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAdamantanoneHCID 64151—
ReactantHCID 54307205HCID 54307205—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 67919426HCID 6791942641.7%

Reaction Steps

20 ml (31 mmol) of a 1.55 molar solution of n-butyllithium in hexane were added dropwise to a solution of 3.03 g (15 mmol) of (3-dimethylaminobenzyl)-imidazole and 1.75 g (15 mmol) of TMEDA in 30 ml of absolute THF. Stirring was carried out for 1 hour at -70° C., after which a solution of 2.26 g of adamantanone in 40 ml of absolute THF was added dropwise at -30° to -15° C. The mixture was allowed to warm up to room temperature in the course of about 45 minutes and was stirred for a further 2 hours at room temperature, 400 ml of water were added at 10° C., while cooling, and stirring was continued for 15 minutes at 0°-5° C., a crystalline precipitate being formed. This was filtered off under suction, rinsed with hexane and diisopropyl ether and dried in vacuo. 2.20 g (= 41.7% yield) of pure (3-dimethylaminophenyl)-(2-hydroxy-2-adamantyl)-1-imidazolylmethane of melting point 185° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05023357
Source datasetuspto-grants-1991_06
ORD IDord-ff19ca17d666438bbb562088024d26ef
Source noteuspto-grants-1991_06