HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383482Erstellt: 25. Oktober 2026
Triethylamine → 2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate
https://huagongshe.com/reaction/383482
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Edukt | 4-Hydroxy-5,5-dimethyl-2(5H)-furanone | HCID 54720139 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate | HCID 58926348 | 89% |
Reaktionsschritte
To a −78° C. stirred solution of 4-hydroxy-5,5-dimethyl-5H-furan-2-one (250 mg, 1.95 mmol) in 18 mL of anhydrous CH2Cl2, was added triethylamine (0.40 mL, 2.9 mmol) and Tf2O (0.49 mL, 2.9 mmol). The reaction was stirred at −78° C. for 30 minutes, and quenched with saturated NH4Cl solution (10 mL). The mixture was warmed up to room temperature and separated. The aqueous layer was extracted with CH2Cl2 (2×20 mL). All organic layers were combined, dried over Na2SO4 and evaporated to brown oil, which was purified by plugging through a short pad of silica gel column with EtOAc/hexanes (1/3). Evaporation of solvents gave 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate as a light brown oil (450 mg, 89%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367664B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-5991e68c395a48ea8b9586856d436e16 |
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| Quellennotiz | uspto-grants-2013_02 |
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