HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268978Generated: October 30, 2026
tert-Butyldimethylsilyl chloride → HCID 54418023, compound
https://huagongshe.com/reaction/2268978
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | (S)-5-Bromo-3-((1-methylpyrrolidin-2-YL)methyl)-1H-indole | HCID 25272002 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54418023 | HCID 54418023 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329390B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-c0ced1bf0ae943769994578b186ea2c8 |
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| Source note | uspto-grants-2001_12 |
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