Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(propan-2-yl)silanethiolHCID 3435097—
ReactantBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 69025407HCID 69025407—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 69023603HCID 69023603—

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629473B2
Source datasetuspto-grants-2009_12
ORD IDord-bc8f80688e124ecfb5dfb5baece01b18
Source noteuspto-grants-2009_12