HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541205Generated: November 1, 2026
(Bis(2-methoxyethyl)amino)sulfur trifluoride → HCID 68288303, compound
https://huagongshe.com/reaction/541205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| Reactant | HCID 68288835 | HCID 68288835 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68288303 | HCID 68288303 | 39.8% |
Reaction Steps
To a solution of tert-butyl 4-(5-cyanopyridin-2-yl)-4-hydroxypiperidine-1-carboxylate (compound 26.2, 1 g, 3.13 mmol, 1.00 equiv, 95%) in dichloromethane (50 mL) under nitrogen at −78° C. was added dropwise a solution of bis(2-methoxyethyl)aminosulfur trifluoride (830 mg, 3.75 mmol, 1.20 equiv) in dichloromethane (10 mL) during the course of 1 min. The resulting mixture was stirred for 1 h at −78° C. The reaction was then carefully quenched by dropwise addition of water and washed with 2×20 mL of sodium bicarbonate(aq) followed by 3×20 mL of brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:10) to yield 0.38 g (38%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871790B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3a69f528d7c340fc80fc0219e72f09c7 |
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| Source note | uspto-grants-2014_10 |
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