HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493099Generated: October 27, 2026
Tris(propan-2-yl)silanethiol → 5-Methyl-2-triisopropylsilanylsulfanyl-benzoic acid methyl ester
https://huagongshe.com/reaction/493099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| Reactant | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Reactant | Methyl 2-bromo-5-methylbenzoate | HCID 15110996 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Methyl-2-triisopropylsilanylsulfanyl-benzoic acid methyl ester | HCID 68897667 | — |
Reaction Steps
2-Bromo-5-methyl-benzoic acid methyl ester (2.06 g, 9.00 mmol), tris(dibenzylideneacetone)dipalladium (0) (83 mg, 0.09 mmol), bis(2-diphenylphosphinophenyl)ether (97 mg, 0.18 mmol), sodium tert-butoxide (1.00 g, 10.4 mmol), triisopropylsilanethiol (1.37g, 7.2 mmol) and dry toluene (10 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 150° C. for 30 minutes. Upon cooling the mixture is poured onto a plug of silica and the product is eluted with ethyl acetate-heptane (2:8). This furnishes 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 | US07534791B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-957c6824786e44e19419b8b615b23c46 |
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| Source note | uspto-grants-2009_05 |
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