Propargyl bromide → HCID 53685511, compound

HRID 1390387Notes

Reaction equation

[CH3:1][CH:2]([O:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1)[CH2:3][CH2:4][CH:5]=[C:6]([CH3:8])[CH3:7].[CH2:19](Br)[C:20]#[CH:21]>>[CH2:21]([O:15][C:14](=[O:16])[C:13]1[CH:12]=[CH:11][C:10]([O:9][CH:2]([CH3:1])[CH2:3][CH2:4][CH:5]=[C:6]([CH3:8])[CH3:7])=[CH:18][CH:17]=1)[C:20]#[CH:19]

Participants

Reactant 2

HCID 7842Propargyl bromide

HCID 22749279HCID 22749279, compound

Product 1

HCID 53685511HCID 53685511, compound

Procedure

By utilizing the procedure of Example 8, by reacting p-[(1,5-dimethyl-4-hexenyl)oxy]benzoic acid with propargyl bromide, there is obtained p-[(1,5-dimethyl-4-hexenyl)oxy]benzoic acid propargyl ester; nD22 = 1.5252.

Sources & evidence

ORD record: ord-625611e5adc24108856fd3da1bdaf9a3
Source dataset: uspto-grants-1979_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04138579

Reaction notes

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