1,4-Dibromobutane → HCID 15170010, compound
Reaction equation
[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([O:10][C:11](=[O:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:4][C:3]1([CH3:31])[CH3:30].[H-].[Na+].Br[CH2:35][CH2:36][CH2:37][CH2:38]Br>O1CCCC1>[C:11]([O:10][CH:5]1[CH2:6][C:7]([CH3:8])([CH3:9])[N:2]([O:1][CH2:35][CH2:36][CH2:37][CH2:38][O:1][N:2]2[C:7]([CH3:8])([CH3:9])[CH2:6][CH:5]([O:10][C:11](=[O:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:4][C:3]2([CH3:30])[CH3:31])[C:3]([CH3:30])([CH3:31])[CH2:4]1)(=[O:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared by reaction of a tetrahydrofuran solution of 1-hydroxy-4-octadecanoyloxy-2,2,6,6-tetramethylpiperidine with sodium hydride followed by reaction with 0.5 molar equivalent of 1,4-dibromobutane.
Sources & evidence
- ORD record
- ord-7ce7e9c9143e418fb1638a74da1cbc37
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05021577
Reaction notes
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