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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883950Generated: October 26, 2026

Potassium triisopropylsilanethiolate → 5-Triisopropylsilanylsulfanyl-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/883950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium triisopropylsilanethiolateHCID 11085560—
Reactant5-Iodo-1H-indole, N-BOC protectedHCID 16125958—
SolventTetrahydrofuranHCID 8028—
Product5-Triisopropylsilanylsulfanyl-indole-1-carboxylic acid tert-butyl esterHCID 6704034889%

Reaction Steps

A solution of the product of Example 59A (200 mg, 0.583 mmol) in anhydrous tetrahydrofuran (4 mL) under a nitrogen atmosphere was treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium methylene chloride complex (5 mg) and the solution was sparged with nitrogen for several minutes. Potassium triisopropylsilanethiolate (146.5 mg, 0.6411 mmol), prepared according to Tetrahedron Letters 35 (20) 3221 1994, was added and the reaction was heated at reflux for 15 minutes. The reaction was cooled to room temperature and the solvent removed by rotary evaporation under vacuum to provide the title compound as a colorless oil (210 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236950B2
Source datasetuspto-grants-2012_08
ORD IDord-46c7a3ed112d49d8b750db64fa1c2a44
Source noteuspto-grants-2012_08