4-Nitrophenol → 2-[(4-Nitrophenoxy)methyl]quinoline

HRID 4373

Reaction equation

HRID 4373 reaction equation

[CH:1]1[C:6]([N+:7]([O-:9])=[O:8])=[CH:5][CH:4]=[C:3]([OH:10])[CH:2]=1.[C:11]1(O)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[N+:7]([C:6]1[CH:5]=[CH:4][C:3]([O:10][CH2:1][C:6]2[CH:5]=[CH:4][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:7]=2)=[CH:2][CH:1]=1)([O-:9])=[O:8]

Participants

3

Reactant 2

HCID 9804-Nitrophenol

Product 1

HCID 137703602-[(4-Nitrophenoxy)methyl]quinoline

Procedure

This compound was prepared in an identical manner as described in Example 1, except p-nitrophenol was substituted for phenol, m.p. 142°-143° C.

Workup

customThis compound was prepared in an identical manner

Sources & evidence

ORD record: ord-69d6dd0a63e846cc9ea6cbd2d9d2af27
Source dataset: uspto-grants-1988_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04725619

Linked notes

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