Propargyl bromide → HCID 22749295, compound

HRID 1390399Notes

Reaction equation

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

Participants

Reactant 2

HCID 7842Propargyl bromide

HCID 53649743HCID 53649743, compound

Product 1

HCID 22749295HCID 22749295, compound

Procedure

By utilizing the procedure of Example 26, by reacting p-[(1,5-dimethylhexyl)thio]benzyl alcohol with propargyl bromide, there is obtained p-[(1,5-dimethylhexyl)thio]-α-propargyloxy-toluene; nD29 = 1.5243.

Sources & evidence

ORD record: ord-1f2fb5566b8944c0963a28005fc0cbe9
Source dataset: uspto-grants-1979_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04138579

Reaction notes

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