Ethyl arachidonate → HCID 86733779, compound
Reaction equation
[CH3:1][CH:2]([CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12]/[CH:13]=[CH:14]\[CH2:15]/[CH:16]=[CH:17]\[CH2:18]/[CH:19]=[CH:20]\[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[C:26](OCC)(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC>>[CH3:1][C:2]([CH3:26])([CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12]/[CH:13]=[CH:14]\[CH2:15]/[CH:16]=[CH:17]\[CH2:18]/[CH:19]=[CH:20]\[CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C:3]([O:5][CH2:6][CH3:7])=[O:4]Participants
3
Procedure
The ethyl 2-methylarachidonate produced in Example 1 is substituted for the ethyl arachidonate in Example 1 and the procedure of Example 1 is repeated to afford ethyl 2,2-dimethylarachidonate. That compound is represented structurally by the following formula ##SPC3##
Sources & evidence
- ORD record
- ord-1a322d1c1b854a3c98f8dac9ec138059
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03972907
Reaction notes
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