HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866801Generated: October 30, 2026
Tris(propan-2-yl)silanethiol → HCID 69023603, compound
https://huagongshe.com/reaction/1866801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| Reactant | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 69025407 | HCID 69025407 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69023603 | HCID 69023603 | — |
Reaction Steps
[2-(2-Bromo-5-fluoro-phenyl)-ethyl]-methyl-carbamic acid tert-butyl ester (3.0 g, 9.03 mmol), tris(dibenzylideneacetone)dipalladium (0) (83 mg, 0.09 mmol), bis(2-diphenylphosphinophenyl)ether (97 mg, 0.18 mmol), sodium tert-butoxide (1.10 g, 11.7 mmol), triisopropylsilanethiol (1.90 g, 9.93 mmol) and dry toluene (15 mL) are all placed in an Emrys Optimizer EXP 20 mL microwave reactor tube. The reaction vessel is sealed and subjected to microwave heating at 160° C. for 15 minutes. Upon cooling the mixture is poured onto a plug of silica and the product is eluted with ethyl acetate-heptane (1:10). This furnishes 1.6 g (40%) of the title compound as an oil, which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629473B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-bc8f80688e124ecfb5dfb5baece01b18 |
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| Source note | uspto-grants-2009_12 |
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