Butyl bromide → HCID 49824264, compound

Reaction equation

[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:15])[CH2:9][N:10]2[N:14]=[N:13][CH:12]=[N:11]2)=[CH:4][CH:3]=1.[CH2:16](Br)[CH2:17][CH2:18][CH3:19]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([O:15][CH2:16][CH2:17][CH2:18][CH3:19])=[CH:9][N:10]2[N:14]=[N:13][CH:12]=[N:11]2)=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 8002Butyl bromide

HCID 132894511-(4-Chlorophenyl)-2-tetrazol-2-yl-ethanone

Product 1

HCID 49824264HCID 49824264, compound

Procedure

Analogously to Example 7a,b, after reacting 1-(4-chlorophenyl)-2-tetrazol-2-yl-ethanone with n-butyl bromide there was obtained 2-[2-(4-chloro-phenyl)-2-butoxy-vinyl]-2H-tetrazole as a colourless oil. [M+H]+=279.

Sources & evidence

ORD record: ord-c48c771c6b2e4272a52460b34c736ef2
Source dataset: uspto-grants-2001_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06248901B1

Reaction notes

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