4-Cyanophenol → HCID 13450886, compound

HRID 544606Notes

Reaction equation

HRID 544606 reaction equation
[K].[C:2]([C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)#[N:3].[Br:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]Br>>[C:2]([C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][Br:11])=[CH:6][CH:5]=1)#[N:3]

Participants

4

Reactant 3

HCID 130194-CyanophenolHCID 783091,7-DibromoheptaneHCID 5462222Potassium

Product 1

HCID 13450886HCID 13450886, compound

Procedure

The intermediate 7-(4-cyanophenoxy)heptyl bromide was prepared from the potassium salt of 4-cyanophenol and 1,7-dibromoheptane.

Sources & evidence

ORD record
ord-c99cf3f886ef411e9f7141c5c4eb4897
Source dataset
uspto-grants-1984_05
Patent number
US04451476

Reaction notes

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