Hexane → HCID 21658117, compound

HRID 374082Notes

Reaction equation

HRID 374082 reaction equation
[CH2:1]([Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7])[CH2:2][CH2:3][CH3:4].[CH3:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]>>[CH2:1]([Si:5]([O:10][CH3:11])([O:6][CH3:7])[O:8][CH3:9])[CH2:2][CH2:3][CH3:4].[CH3:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]

Participants

3

Conditions

Temperature
0 °C

Procedure

In a separate reaction vessel under nitrogen, 5.0 ml n-butyl(trimethoxy)silane (0.026 mol.) was added along with 50 ml hexane. The vessel was cooled to 0° C. in an ice bath while stirring. To the cooled n-butyl(trimethoxy)silane/hexane solution obtained was added, via cannula, 2.68 g 1-lithio-4-methylpiperidine suspension from the first vessel. After the addition was completed, the reaction mixture was allowed to warm to room temperature, stirred for about 16 hours, then heated to reflux for about 2 hours. The solvents were then removed in vacuo and the white solid was washed 3 times with 20 ml portions of hexane to remove the product. The hexane was stripped from the product under vacuum to give an oil.

Workup

  1. customIn a separate reaction vessel under nitrogen

Sources & evidence

ORD record
ord-f24b1e2478864f988f541b90b84f600d
Source dataset
uspto-grants-1992_11
Patent number
US05166340

Reaction notes

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