HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215954Generated: November 2, 2026
Acetic Acid → 4-Azido-5-ethoxy-dihydrofuran-2-one
https://huagongshe.com/reaction/2215954
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 5-Ethoxy-5H-furan-2-one | HCID 3293575 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Azido-5-ethoxy-dihydrofuran-2-one | HCID 11298209 | 73% |
Reaction Steps
This procedure was carried out in a manner similar to that described by D. J. Guerin, et al., Org. Lett (1999), 1, 1107-1109. To a solution of azidotrimethylsilane (25.8 mL, 0.32 mol) in dichloromethane (400 mL) at room temperature under nitrogen was added acetic acid (18.1 mL, 0.32 mol), and the reaction was stirred for 20 min. 5-Ethoxy-5H-furan-2-one (II, R1=Et) (8.10 g, 0.063 mol) was added dropwise, followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (1.9 mL, 0.013 mol). The reaction was stirred for 24 h, washed with sodium bicarbonate, dried over sodium sulfate and evaporated. Purification by flash chromatography (SiO2) eluted with 1:9 ethyl acetate:hexanes afforded 4-azido-5-ethoxy-dihydrofuran-2-one (7.85 g, 73% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109357B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-aeab2a383ca34c59975c00ec82c08698 |
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| Source note | uspto-grants-2006_09 |
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