Water → HCID 86740303, compound
Reaction equation
[CH2:1]([C:13]12[S:20][C:14]1([OH:19])[CH:15]=[CH:16][CH:17]=[CH:18]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[B:21]([OH:24])([OH:23])[OH:22].O>C1(C)C=CC=CC=1>[O:19]1[CH:15]([CH2:16][CH2:17][CH2:18][CH2:13][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH2:14]1.[B:21]([OH:24])([OH:23])[OH:22].[CH2:1]([C:13]12[S:20][C:14]1([OH:19])[CH:15]=[CH:16][CH:17]=[CH:18]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Approximately 60 g of 1,2-epoxyhexadeacane (obtained from Union Carbide Co.), 135 g of 50% dodecylphenol sulfide (made by reacting 3 moles of dodecylphenol with 2 moles of sulfur dichloride at 100° to 150° C. for 6 hours with agitation followed by vacuum topping to remove residual HCl) in 100" solvent paraffinic neutral lubricating diluent oil, 100 g of toluene solvent and 20 g of boric acid were charged to a reactor equipped with agitator, heater, Dean-Start tube with condenser and provision for maintaining an inert nitrogen atmosphere. The reactor contents were heated up to 170° C. over a period of 6 hours until water evolution ceased. The solvent was removed by distillation under reduced pressure and the product was then filtered through diatomaceous earth.
Workup
- customequipped with agitator, heater, Dean-Start tube with condenser
- temperatureprovision for maintaining an inert nitrogen atmosphere
- customThe solvent was removed by distillation under reduced pressure
- filtrationthe product was then filtered through diatomaceous earth
Sources & evidence
- ORD record
- ord-91d71601c4d54b2c89969ab494a2cb16
- Source dataset
- uspto-grants-1985_09
- Patent number
- US04541942
Reaction notes
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