HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108787Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 14612530, compound
https://huagongshe.com/reaction/2108787
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86600237 | HCID 86600237 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14612530 | HCID 14612530 | — |
Reaction Steps
(3R,4R)-3-Azidomethyl-1-benzyl-4-hydroxypyrrolidine (566 mg) was dissolved in dichloromethane (9 mL). While this solution was chilled in an ice water bath, diethylaminosulfur trifluoride (0.39 mL) was added dropwise and the mixture was stirred at room temperature for 2 hours. While the reaction vessel was chilled in an ice water bath, a saturated aqueous solution of sodium bicarbonate (9 mL) was added and the mixture was diluted with dichloromethane (15 mL). The dichloromethane layer was separated, washed sequentially with a saturated aqueous solution of sodium bicarbonate (10 mL) and water (10 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluant: hexane: ethyl acetate=4:1). The first half fraction yielded (3R,4R)-3-azidomethyl-1-benzyl-4-fluoropyrrolidine as a pale brown oil (76.7 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514451B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-f595ee5e5e1944e4a04b80c63523d5fc |
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| Source note | uspto-grants-2009_04 |
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