HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197608Generated: October 29, 2026
(Diethylamino)sulfur trifluoride → HCID 15690213, compound
https://huagongshe.com/reaction/1197608
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 11074181 | HCID 11074181 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 15690213 | HCID 15690213 | 65% |
Reaction Steps
To a stirring solution of 3-azido-2-hydroxypropanal diethyl acetal (7.32 g, 38.73 mmol) in dry benzene (50 mL) was added diethylaminosulfurtrifluoride (DAST; 20.6 mL) at -78° C. After the addition, the solution was stirred at room temperature for an hour, then heated to 70° C. for 12 hours. The reaction was quenched by the addition of methanol at zero degrees C. and dilution with water. After dichloromethane extraction, the organic layer was dried over MgSO4 and concentrated in vacuo. The crude product was purified with silica gel column chromatography (hexane: ether=9:1, volume/volume) to yield 3-azido-2-fluoropropanal diethyl acetal as an oil (65 percent); Rf =0.84 EtOAc:hexane=2:3) 1H-NMR (CD3Cl) δ 1.215~1.219 (6H, m) 3.526 (2H, dm, J=15.3 Hz), 3.642~3.670 (2H, m), 3.680~3.808 (2H, m), 4.514 (1H, dm, J=45.9 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05276120 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-b4db1d0595264269be6d76b798bad519 |
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| Source note | uspto-grants-1994_01 |
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