3,4-Dichloro-1-butene → HCID 10999815, compound
Reaction equation
[Cl:1][SiH:2]([Cl:4])[Cl:3].[CH2:5]=[CH:6][CH:7]([Cl:10])[CH2:8][Cl:9]>>[Cl:10][CH:7]([CH2:8][Cl:9])[CH2:6][CH2:5][Si:2]([Cl:4])([Cl:3])[Cl:1]Participants
3
Procedure
596 g trichlorosilane (4.4 moles, excess) and 500 g 3,4-dichlorobutene-1 (4 moles) are mixed. 0.4 g Pt(II)-acetyl acetonate are added to 30 ml of this mixture, at which time the temperature gradually rises by itself to 95° C. At this temperature, the remaining trichlorosilane/olefin mixture is added and allowed to react for an additional half hour at 92° C. Excess trichlorosilane and other readily volatile constituents are drawn off in a vacuum. The crude product obtained in this manner (826 g ≅79.3 % of theory) is subsequently purified by distillation. 705 g 3,4-dichlorobutyl trichlorosilane≅7 % of theory are obtained as the main fraction (see table 1 for composition data).
Workup
- customgradually rises by itself to 95° C
- customto react for an additional half hour at 92° C
- customThe crude product obtained in this manner (826 g ≅79.3 % of theory)
- distillationis subsequently purified by distillation
Sources & evidence
- ORD record
- ord-5bfe58b16a8848eb9bbb1e7a89fd8a83
- Source dataset
- uspto-grants-1992_11
- Patent number
- US05164501
Reaction notes
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