Potassium Hydroxide → HCID 53241517, compound

HRID 2205271Notes

Reaction equation

HRID 2205271 reaction equation
[OH-].[K+].[CH3:3][N:4]([CH3:10])[CH2:5][CH:6]([OH:9])[CH2:7]O.CS([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26]/[CH:27]=[CH:28]\[CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])(=O)=O>CC1CCCCC1>[CH2:16]([O:15][CH:5]([N:4]([CH3:10])[CH3:3])[CH:6]([O:9][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26]/[CH:27]=[CH:28]\[CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[CH3:7])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]/[CH:24]=[CH:25]\[CH2:26]/[CH:27]=[CH:28]\[CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]

Participants

5

Reactant 3

HCID 14797Potassium HydroxideHCID 790783-(Dimethylamino)-1,2-propanediolHCID 59753235Linoleyl methanesulfonate

Product 1

HCID 53241517HCID 53241517, compound

Reagents, catalysts & solvents 1

HCID 7962MethylcyclohexaneSolvent

Procedure

In a nitrogen atmosphere, methylcyclohexane (30 mL) and potassium hydroxide (3.1 g, 54.4 mmol) were added to a four-necked flask, and 3-(dimethylamino)-1,2-propanediol (0.72 g, 6.04 mmol: DAP) was dropped under agitation. Thereafter, linoleyl methane sulfonate (5.0 g, 14.5 mmol) was added, and agitation was performed at 40° C. for 13 hours. The reaction was terminated because remaining linoleyl methane sulfonate became 2.1% (degree of conversion: 68.0%, integrated value of isomer: 0.024).

Workup

  1. customThe reaction was terminated

Sources & evidence

ORD record
ord-62972af100a944f4a43cb34480a5e43d
Source dataset
uspto-grants-2016_06
Patent number
US09371271B2

Reaction notes

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