Diethyl Ether → HCID 58827413, compound

HRID 2378141Notes

Reaction equation

[C:1]1([CH3:22])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[N:9]=[CH:10][CH:11]=[N:12][C:13]1[C:18]([CH3:19])=[CH:17][C:16]([CH3:20])=[CH:15][C:14]=1[CH3:21].[CH2:23]([Li])[CH2:24][CH2:25][CH3:26].[CH3:28][CH2:29][CH2:30][CH2:31]CC.C(OCC)C>C1COCC1.O>[C:1]1([CH3:22])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[NH:9][CH:10]([CH:11]([NH:12][C:13]1[C:14]([CH3:21])=[CH:15][C:16]([CH3:20])=[CH:17][C:18]=1[CH3:19])[CH2:28][CH2:29][CH2:30][CH3:31])[CH2:23][CH2:24][CH2:25][CH3:26]

Participants

Conditions

Temperature: -78 °C

Procedure

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%).

Workup

temperatureThe reaction mixture was warmed to −10° C. over a period of one hour
extractionThe aqueous layer was extracted with 2×5 ml of ether
customthe combined extracts were dried
waitleft an orange oil
customThe crude product was chromatographed on a silica gel column (50 g)
washeluted with petroleum ether/toluene (1:1)

Sources & evidence

ORD record: ord-7b69dc1422c74450ae8ec797bd949ee3
Source dataset: uspto-grants-2008_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07470750B2

Reaction notes

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