HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272698Generated: November 2, 2026
Methanesulfonyl chloride → HCID 86596594, compound
https://huagongshe.com/reaction/1272698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 86596595 | HCID 86596595 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86596594 | HCID 86596594 | — |
Reaction Steps
Tetrakis(bromopropyldimethylsiloxy)silane was synthesized by the following reactions starting from tetrakis(dimethylsiloxy)silane. Thus, allyloxytrimethylsilane was reacted with tetrakis(dimethylsiloxy)silane in the presence of a platinum 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex as catalyst to produce tetrakis(trimethylsiloxypropyldimethylsiloxy)silane, from which the trimethylsiloxy group was subsequently eliminated by the action of excess methanol to give tetrakis(hydroxypropyldimethylsiloxy)silane. Methanesulfonyl chloride was then reacted in pyridine with the tetrakis(hydroxypropyldimethylsiloxy)silane to give tetrakis(methanesulfonyloxypropyldimethylsiloxy)silane, which was subsequently reacted with sodium bromide in DMF to give tetrakis(bromopropyldimethylsiloxy)silane:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208561B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-a88c3c120c9d4ae4a8555fe1cc3d6a52 |
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| Source note | uspto-grants-2007_04 |
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