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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(propan-2-yl)silanethiolHCID 3435097—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
ReactantMethyl 2-bromo-5-methylbenzoateHCID 15110996—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product5-Methyl-2-triisopropylsilanylsulfanyl-benzoic acid methyl esterHCID 68897667—

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534791B2
Source datasetuspto-grants-2009_05
ORD IDord-957c6824786e44e19419b8b615b23c46
Source noteuspto-grants-2009_05