1-Bromo-3-methylbutane → HCID 18963351, compound

HRID 359314Notes

Reaction equation

HRID 359314 reaction equation
[C:1]([C:4]1[CH2:9][CH2:8][CH2:7][NH:6][CH:5]=1)(=[O:3])[CH3:2].Br[CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14].CC(N1CCCC(C(C)=O)=C1)C>>[CH3:14][CH:13]([CH3:15])[CH2:12][CH2:11][N:6]1[CH2:7][CH2:8][CH2:9][C:4]([C:1]([CH3:2])=[O:3])=[CH:5]1

Participants

4

Reactant 3

HCID 78911-Bromo-3-methylbutaneHCID 32845951-(1,4,5,6-tetrahydropyridin-3-yl)ethanoneHCID 18963350HCID 18963350, compound

Product 1

HCID 18963351HCID 18963351, compound

Procedure

Methyl 1-(3-methylbutyl)-1,4,5,6-tetrahydro-3-pyridyl ketone was prepared from 3-acetyl-1,4,5,6-tetrahydropyridine and 1-bromo-3-methylbutane according to the procedure of Part (b) of Example 1. The product distilled as a pale yellow oil (b.pt. 103-106 °C./0.1 mm Hg).

Workup

  1. distillationThe product distilled as a pale yellow oil (b.pt. 103-106 °C./0.1 mm Hg)

Sources & evidence

ORD record
ord-f973e796cb4045f896c34b9855b760c9
Source dataset
uspto-grants-1991_03
Patent number
US05000946

Reaction notes

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