Isopropanol → Tert-butyl 2-bromo-2-(diethoxyphosphoryl)acetate
Reaktionsgleichung
[CH2:1]([O:3][P:4]([C:9](Br)([Br:17])[C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])([O:6][CH2:7][CH3:8])=[O:5])[CH3:2].C(O)(C)C.[Sn](Cl)Cl>O>[CH2:1]([O:3][P:4]([CH:9]([Br:17])[C:10]([O:12][C:13]([CH3:14])([CH3:16])[CH3:15])=[O:11])([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Combine t-butyl diethylphosphonodibromoacetate (75.6 g, 184 mmol) and isopropanol (190 mL). Cool to 0° C. Add a solution of tin (II) chloride (33.2 g, 175 mmol) in water (190 mL). After the addition is complete, warm to ambient temperature. After 1 hour, extract the reaction mixture three times with chloroform. Combine the organic layers and extract with water, dry over MgSO4, filter, and evaporate in vacuo to give the title compound.
Aufarbeitung
- additionAfter the addition
- temperaturewarm to ambient temperature
- extractionextract the reaction mixture three times with chloroform
- extractionextract with water
- dry with materialdry over MgSO4
- filtrationfilter
- customevaporate in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-6567ebc10bb04297a2fee93a840de8d8
- Quelldatensatz
- uspto-grants-1996_10
- Patentnummer
- US05563157
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