Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | cis,cis-1,5-Cyclooctadiene | HCID 8135 | — |
| Reactant | Silane | HCID 23953 | — |
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Product | Allyl chloride | HCID 7850 | — |
| Product | Silane, chloro(3-chloropropyl)dimethyl- | HCID 82765 | — |
Reaction Steps
Dimethylchlorosilane as one feed stream and a mixture of 2.7×10−3 mol % of di-μ-chlorobis[(cycloocta-1c,5c-diene)iridium(I)] and 7×10−1 mol % of 1,5-cyclooctadiene in allyl chloride as a second feed stream were fed in a molar ratio of silane:allyl chloride mixture of 1:1.05 at a rate of 2.8 l/h (based on the total volume of the components introduced) via separate metering pumps into a loop reactor maintained at 80° C. under a pressure of 0.4 MPa and having a volume of 1.4 l. After working up the crude mixture by distillation using a thin film evaporator to separate off the catalyst and the excess of allyl chloride, chloro(3-chloropropyl)dimethylsilane was obtained in a yield of 95% and a purity of >99% based on the silane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208618B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-a30623f571334f4fbae743e59d7e8373 |
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| Source note | uspto-grants-2007_04 |
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