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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378141Generated: November 1, 2026

Diethyl Ether → HCID 58827413, compound

https://huagongshe.com/reaction/2378141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHexaneHCID 8058—
ReactantBenzenamine, N,N'-1,2-ethanediylidenebis[2,4,6-trimethyl-, [N(E),N'(E)]-HCID 3741651—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58827413HCID 5882741365%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a 150 ml Schlenk vessel, N,N′-dimesitylethanediimine (2.92 g; 10 mmol) was dissolved in 30 ml of THF under nitrogen as protective gas and the solution was cooled to −78° C. 1.6 M Butyllithium in hexane (13.8 ml; 22 mmol) was then slowly added to the resulting suspension at −78 ° C. The reaction mixture was warmed to −10° C. over a period of one hour and was stirred at this temperature for a further hour. The solvent was then taken off and 15 ml of diethyl ether and 10 ml of water were then added on an ice bath. The aqueous layer was extracted with 2×5 ml of ether and the combined extracts were dried over powdered NaOH. Taking off the solvent left an orange oil. The crude product was chromatographed on a silica gel column (50 g) and eluted with petroleum ether/toluene (1:1). Taking off the solvent gave yellow crystals of dl-N,N′-dimesityldecane-5,6-diamine (2.67 g; 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470750B2
Source datasetuspto-grants-2008_12
ORD IDord-7b69dc1422c74450ae8ec797bd949ee3
Source noteuspto-grants-2008_12