Propargyl bromide → HCID 54253596, compound

HRID 1390386Notes

Reaction equation

[CH2:1]([O:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([OH:23])=[O:22])=[CH:19][CH:18]=1)[CH:2]=[C:3]([CH2:5][CH2:6][CH:7]=[C:8]([CH2:10][CH2:11][CH:12]=[C:13]([CH3:15])[CH3:14])[CH3:9])[CH3:4].[CH2:26](Br)[C:27]#[CH:28]>>[CH2:28]([O:22][C:21](=[O:23])[C:20]1[CH:19]=[CH:18][C:17]([O:16][CH2:1][CH:2]=[C:3]([CH2:5][CH2:6][CH:7]=[C:8]([CH2:10][CH2:11][CH:12]=[C:13]([CH3:14])[CH3:15])[CH3:9])[CH3:4])=[CH:25][CH:24]=1)[C:27]#[CH:26]

Participants

Reactant 2

HCID 7842Propargyl bromide

HCID 54420520HCID 54420520, compound

Product 1

HCID 54253596HCID 54253596, compound

Procedure

By utilizing the procedure of Example 8, by reacting p-farnesyloxybenzoic acid with propargyl bromide, there is obtained p-farnesyloxybenzoic acid propargyl ester; B.P. 245°-250° C./0.1 mmHg.

Sources & evidence

ORD record: ord-596148f01d784912971f3405532164b8
Source dataset: uspto-grants-1979_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04138579

Reaction notes

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