HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048178Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 13616595, compound
https://huagongshe.com/reaction/1048178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 11403074 | HCID 11403074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13616595 | HCID 13616595 | 89.8% |
Reaction Steps
To a solution of 2-(2,4-dichlorophenyl)-2-(trimethylsilyloxy)acetonitrile (1.57 g, 5.73 mmol) in dichloromethane (20 ml) under argon at −78° C. was added (diethylamino)sulfur trifluoride (1.51 ml, 11.5 mmol) dropwise over 15 minutes. The reaction was stirred at this temperature for 20 minutes, then warmed to 0° C. and allowed to stir for an additional 30 minutes. The reaction was poured onto a mixture of ice water and saturated sodium bicarbonate and allowed to stir for 30 minutes. The mixture was extracted with ether twice, and the combined organic layers were washed with saturated sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated to yield 1.05 g of the title compound (89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569522B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0ffe2530f57c4980b9c3f0e76042970f |
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| Source note | uspto-grants-2013_10 |
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