HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170438Generated: November 3, 2026
(Diethylamino)sulfur trifluoride → HCID 178464129, compound
https://huagongshe.com/reaction/1170438
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178464135 | HCID 178464135 | — |
| Product | HCID 178464129 | HCID 178464129 | 85.8% |
Reaction Steps
To the compound of Example 1-4 (150.0 mg, 0.26 mmol) was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was dissolved in dichloromethane (2.6 mL), and thereto was added diethylaminosulfur trifluoride (207.9 mg, 1.29 mmol) at −78° C., and the mixture was allowed to warm to room temperature and stirred for 24 hours. To the reaction solution was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated, and then purified by silica gel column chromatography (chloroform/methanol/ammonia water 20/1/0 to 10/1/0 to 100/10/1), and then by preparative liquid chromatography. To the purified substance were added tetrahydrofuran and 1M hydrochloric acid (0.5 mL), and the mixture was concentrated. The resulting solid was suspended in diethyl ether and filtered to give the titled compound (65.0 mg, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825155B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-a070516f26e34a45a2748b24b5d13176 |
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| Source note | uspto-grants-2010_11 |
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