Reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][Si:5](Cl)([CH3:7])[CH3:6].C(=O)([O-])[O-].[Na+].[Na+].[OH2:15]>>[Cl:1][CH2:2][CH2:3][CH2:4][Si:5]([CH3:7])([CH3:6])[O:15][Si:5]([CH2:4][CH2:3][CH2:2][Cl:1])([CH3:7])[CH3:6]Participants
Procedure
To a triangular flask of 2 l containing 1200 ml of water was added dropwise 342 g of 3-chloropropylchlorodimethylsilane (hereinafter referred to as "CPCDMSi") in an hour while stirring with a magnetic stirrer at a room temperature. After completion of the addition, the reaction mixture was neutralized with sodium carbonate and then extracted three times with each 500 ml of n-hexane. After drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane was removed under reduced pressure. The obtained residue was distilled under reduced pressure, and then the distillate obtained at 103° C./1.5 mmHg was collected to give 255 g (Yield 89%) of 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyldisiloxane (hereinafter referred to as "BCPSi").
Workup
- customin an hour
- additionAfter completion of the addition
- extractionextracted three times with each 500 ml of n-hexane
- dry with materialAfter drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane
- customwas removed under reduced pressure
- distillationThe obtained residue was distilled under reduced pressure
- customthe distillate obtained at 103° C./1.5 mmHg
- customwas collected
Sources & evidence
- ORD record
- ord-183c214edbe94ae8a1b2f00cd9c726de
- Source dataset
- uspto-grants-1985_06
- Patent number
- US04525563
Linked notes
Loading…