Azane;hydrate → 2,6,10,14,18-Pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenamide

HRID 477619Notes

Reaction equation

[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:3](O)=[O:4].O.[NH3:33]>>[CH3:1][C:2](=[CH:6][CH2:7][CH2:8][C:9]([CH3:31])=[CH:10][CH2:11][CH2:12][C:13]([CH3:30])=[CH:14][CH2:15][CH2:16][C:17]([CH3:29])=[CH:18][CH2:19][CH2:20][C:21]([CH3:28])=[CH:22][CH2:23][CH2:24][C:25](=[O:27])[CH3:26])[C:3]([NH2:33])=[O:4]

Participants

Reactant 2

HCID 12896473Azane;hydrate

HCID 538735642,6,10,14,18-Pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoic acid

Product 1

HCID 867436222,6,10,14,18-Pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenamide

Procedure

Starting materials: 2,6,10,14,18-pentamethyl-22-oxo-2,6,10,14,18-tricosapentaenoic acid and ammonia water (28% ammonia water).

Sources & evidence

ORD record: ord-ce9c0f5e463e458fb5115c70b7994cb7
Source dataset: uspto-grants-1989_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04888439

Reaction notes

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