Dimethylamine → HCID 86743078, compound

HRID 1762890Notes

Reaction equation

HRID 1762890 reaction equation
[CH3:1][C:2]([CH:7]=[CH:8][CH:9]=[C:10]([CH3:22])[CH2:11][CH2:12][CH:13]=[C:14]([CH3:21])[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19])=[CH:3][C:4](O)=[O:5].[CH3:23][NH:24][CH3:25]>>[CH3:23][N:24]([CH3:25])[C:4](=[O:5])[CH:3]=[C:2]([CH3:1])[CH:7]=[CH:8][CH:9]=[C:10]([CH3:22])[CH2:11][CH2:12][CH:13]=[C:14]([CH3:21])[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19]

Participants

3

Reactant 2

HCID 674DimethylamineHCID 1147413,7,11,15-Tetramethylhexadeca-2,4,6,10,14-pentaenoic acid

Product 1

HCID 86743078HCID 86743078, compound

Procedure

3,7,11,15-Tetramethyl-2,4,6,10,14 -hexadecapentaenoic acid and dimethylamine were reacted in the same manner as in Preparation Example 9 to obtain the desired product as pale yellow crystals.

Sources & evidence

ORD record
ord-0b09fb97e61048188d42e6caa309260e
Source dataset
uspto-grants-1989_05
Patent number
US04835183

Reaction notes

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