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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268978Generated: October 30, 2026

tert-Butyldimethylsilyl chloride → HCID 54418023, compound

https://huagongshe.com/reaction/2268978

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(S)-5-Bromo-3-((1-methylpyrrolidin-2-YL)methyl)-1H-indoleHCID 25272002—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54418023HCID 5441802379%

Reaction Steps

To a solution of (S)-5-bromo-3-[(N-methylpyrrolidin-2-yl)methyl]-l H-indole (Example 3c, 1.00 g, 3.41 mmol) in THF (15 mL) under argon, was added sodium hexamethyldisilazide (6.82 mL, 6.82 mmol and the resulting solution was stirred at room temperature for 20 min. The reaction mixture was cooled to 0° C. and to this was added a solution of t-butydimethylsilyl chloride (1.03 g, 6.82 mmol) in THF (4 mL) and the resulting culture was warmed to room temperature and stirred for 1 hour. The solvent as removed in vacuo and the resulting product was diluted with water (10 mL) and extracted with ethyl acetate (2×10 mL). The ethyl acetate extract was washed with brine (10 mL), dried (Na2SO4), filtered and the filtrate was evaporated to dryness. The crude residue was subjected to flash silica gel chromography to afford the title compound as a yellow oil (1.07 g, 79%). 13C NMR (CDCl3)δ: 140.1, 133.1, 129.8, 124.1, 121.5, 115.8, 115.2, 112.7, 66.2, 7.6, 40.9, 31.6, 30.1, 26.2, 21.9, 19.5, −3.96

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329390B1
Source datasetuspto-grants-2001_12
ORD IDord-c0ced1bf0ae943769994578b186ea2c8
Source noteuspto-grants-2001_12