Pyridine → HCID 131716991, compound

HRID 727751Notes

Reaction equation

[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][O:17][CH2:18][CH2:19][O:20][CH2:21][CH2:22][O:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][O:32][CH2:33][CH2:34][O:35][CH2:36][CH2:37][O:38][CH2:39][CH2:40][OH:41].[N:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1>>[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][O:17][CH2:18][CH2:19][O:20][CH2:21][CH2:22][O:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][O:29][CH2:30][CH2:31][O:32][CH2:33][CH2:34][O:35][CH2:36][CH2:37][O:38][CH2:39][CH2:40][OH:41].[NH+:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1

Participants

Reactant 2

HCID 1049Pyridine

HCID 3625611Hexadecyloctaglycol

Product 1

HCID 131716991HCID 131716991, compound

Procedure

C16E8 -Pyridinium was synthesized by tresylation of C16E8 followed by reaction with pyridine and purification by reverse phase HPLC as described in Examples 1-3 above.

Sources & evidence

ORD record: ord-2b5576aae59843cda27c24e4bd834ff5
Source dataset: uspto-grants-1991_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05045190

Reaction notes

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