Acryloyl chloride → Bis(4-acryloyloxy-2,2,6,6-tetramethylpiperidin-1-yloxy)octane

HRID 1493531Notes

Reaction equation

HRID 1493531 reaction equation
[OH:1][CH:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[N:5]([O:10][CH:11]([O:19][N:20]2[C:25]([CH3:27])([CH3:26])[CH2:24][CH:23]([OH:28])[CH2:22][C:21]2([CH3:30])[CH3:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:4]([CH3:32])([CH3:31])[CH2:3]1.[C:33](Cl)(=[O:36])[CH:34]=[CH2:35]>>[C:33]([O:28][CH:23]1[CH2:22][C:21]([CH3:30])([CH3:29])[N:20]([O:19][CH:11]([O:10][N:5]2[C:6]([CH3:8])([CH3:9])[CH2:7][CH:2]([O:1][C:2](=[O:1])[CH:3]=[CH2:4])[CH2:3][C:4]2([CH3:31])[CH3:32])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:25]([CH3:27])([CH3:26])[CH2:24]1)(=[O:36])[CH:34]=[CH2:35]

Participants

3

Reactant 2

HCID 13140Acryloyl chlorideHCID 23372110Bis(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yloxy)octane

Product 1

HCID 19778495Bis(4-acryloyloxy-2,2,6,6-tetramethylpiperidin-1-yloxy)octane

Procedure

The title compound is prepared by the reaction of the compound prepared in Example 4 with acryloyl chloride.

Sources & evidence

ORD record
ord-3b46a22ea0724b21a0a554676a2243ac
Source dataset
uspto-grants-1991_06
Patent number
US05021577

Reaction notes

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