HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium triisopropylsilanethiolate → 5-Triisopropylsilanylsulfanyl-indole-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium triisopropylsilanethiolate | HCID 11085560 | — |
| Reactant | 5-Iodo-1H-indole, N-BOC protected | HCID 16125958 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Triisopropylsilanylsulfanyl-indole-1-carboxylic acid tert-butyl ester | HCID 67040348 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236950B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-46c7a3ed112d49d8b750db64fa1c2a44 |
| Source note | uspto-grants-2012_08 |