3,4-Dichloro-1-butene → HCID 10999815, compound

HRID 1461106Notes

Reaction equation

HRID 1461106 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 67.7% of theory are obtained as the main fraction (see table 1 for composition data).

Workup

  1. customgradually rises by itself to 95° C
  2. customto react for an additional half hour at 92° C
  3. customThe crude product obtained in this manner (826 g≅79.3% of theory)
  4. distillationis subsequently purified by distillation

Sources & evidence

ORD record
ord-91b758a1ec50492b909fea8874cc8718
Source dataset
uspto-grants-1991_12
Patent number
US05073644

Reaction notes

Loading…