1-Bromo-3-methylbutane → HCID 18963387, compound

Reaction equation

[CH3:1][C:2]1([CH3:12])[CH2:11][C:10]2[NH:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3]1.Br[CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17].CC(N1CCCC(C(C)=[O:29])=C1)C>>[CH3:1][C:2]1([CH3:12])[CH2:11][C:10]2[N:9]([CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17])[CH2:8][CH2:7][CH2:6][C:5]=2[C:4](=[O:29])[CH2:3]1

Participants

Reactant 3

HCID 78911-Bromo-3-methylbutane

HCID 18963350HCID 18963350, compound

HCID 18963386HCID 18963386, compound

Product 1

HCID 18963387HCID 18963387, compound

Procedure

7,7-Dimethyl-1,2,3,4,7,8-hexahydro-quinolin- (5(6H)-one was reacted with 1-bromo-3-methylbutane according to the procedures of Part (b) of Example 1 to give 7,7-dimethyl-1,2,3,4,7, 8-hexahydro-1-(3-methylbutyl)-quinolin-5(6H)one (18) as a pale yellow oil.

Sources & evidence

ORD record: ord-6a275d173b8647b2853b655df3ba6551
Source dataset: uspto-grants-1991_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05000946

Reaction notes

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