Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Bis(chlorodimethylsilyl)ethane | HCID 83552 | — |
| Reactant | 2,4-Difluorobenzylamine | HCID 2733244 | — |
| Reactant | Triethylazanium chloride | HCID 12698378 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19980941 | HCID 19980941 | — |
Reaction Steps
107.6 g (0.05 mol) of 1,2-bis(chlorodimethylsilyl)ethane are introduced into 200 ml of dichloromethane. A solution of 71.6 g (0.50 mol) of 2,4-difluorobenzylamine and 101.2 g (1.0 mol) of triethylamine in 300 ml of dichloromethane are added dropwise at room temperature over the course of 2.5 hours, to give a white suspension. The end of the reaction is checked by gas chromatography. 400 ml of 10% sodium dihydrogen phosphate solution are then added in order to dissolve the precipitated triethylammonium chloride. The organic phase is separated off, dried using magnesium sulfate, filtered and evaporated on a vacuum rotary evaporator. The turbid oil is taken up in 300 ml of petroleum ether, clarified and re-evaporated. 124.7 g of a colourless liquid which is purified by fractional distillation at 125°-127° C. and 15 mbar are obtained. 85.3 g (60% or theory) of pure product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068371 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-8588aa2a0a524025b1cbbe6e141aaaa8 |
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| Source note | uspto-grants-1991_11 |
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