HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 333077Erstellt: 24. Oktober 2026
Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate
https://huagongshe.com/de/reaction/333077
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Methanesulfonate | HCID 6113 | — |
| Edukt | Diethyl chlorophosphate | HCID 13139 | — |
| Edukt | n-Butyl lithium | HCID 61028 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl (diethoxyphosphoryl)methanesulfonate | HCID 10934205 | 117,1% |
Reaktionsschritte
A solution of ethyl methanesulfonate (4.14 mL, 40.2 mmol) in anhydrous tetrahydrofuran (100 ml) was cooled to −78° C. under a nitrogen atmosphere. N-Butyllithium (20 ml, 50.0 mmol) was added slowly in 7 minutes after which stirring was continued for 15 minutes. Diethyl phosphorochloridate (4.36 mL, 30.2 mmol) was added, the reaction mixture was stirred for 2.5 h, the cooling bath was removed and the mixture was allowed to reach room temperature. The reaction mixture was quenched with aqueous saturated ammonium chloride (150 ml) and the resulting mixture was extracted with EtOAc (2×100 ml). The combined extracts were dried over sodium sulfate and concentrated under reduced pressure to yield 9.20 g of a yellow oil. The oil was purified over silicagel (600 g) using a gradient of ethyl acetate (0-100%) in heptane to yield 1.75 g of the product (6.7 mol, 17%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08877934B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-40d13101437a4e78a60ba9d76cfe0aff |
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| Quellennotiz | uspto-grants-2014_11 |
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