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| | Propanoic acid, 2-[bis(2,2,2-trifluoroethoxy)phosphinyl]-, methyl ester Basic information |
| | Propanoic acid, 2-[bis(2,2,2-trifluoroethoxy)phosphinyl]-, methyl ester Chemical Properties |
| Boiling point | 260.0±40.0 °C(Predicted) | | density | 1.418±0.06 g/cm3(Predicted) | | solubility | Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly) | | form | Oil | | color | Colourless to Pale Yellow | | Stability: | Moisture Sensitive |
| | Propanoic acid, 2-[bis(2,2,2-trifluoroethoxy)phosphinyl]-, methyl ester Usage And Synthesis |
| Uses | Methyl 2-[Bis(2,2,2-trifluoroethoxy)phosphinyl]propionate is synthetic reagent used in Z-selective HWE reactions (a.k.a. Still-Genari modification) to make alpha,β-unsaturated esters. Methyl 2-[Bis(2,2,2-trifluoroethoxy)phosphinyl]propionate is used as reagent/reactant for preparation of (±)-(Z)-2β-hydroxy-14-hydro-β-santalol via tandem radical cyclization. | | Synthesis | KHMDS (8.0 mL, 4.00 mmol, 0.5M in toluene) was added by syringe to a
solution of dried 18-crown-6 (4.20 g, 15.89 mmol), THF (20 mL), and Bis (2,2,2-trifluoroethyl) phosphite (0.55
mL, 3.75 mmol) at -78 ℃. Following 15 min, methyl 2-bromopropionate (0.35 mL, 3.14
mmol) was added to the reaction flask. The reaction mixture was allowed to warm to
room temperature for 4hr. The standard workup protocol was followed, then the crude
product was purified by flash column chromatography (9:1-3:2 hexanes:EtOAc, Rf
= 0.22
in 1:1 hexanes:EtOAc) yielding Propanoic acid, 2-[bis(2,2,2-trifluoroethoxy)phosphinyl]-, methyl ester (103 mg, 31 mmol, 9.9%) as a yellow
syrup. |
| | Propanoic acid, 2-[bis(2,2,2-trifluoroethoxy)phosphinyl]-, methyl ester Preparation Products And Raw materials |
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