Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phosphonous dichloride, 1,2-ethanediylbis- | HCID 119904 | — |
| Reactant | HCID 178443133 | HCID 178443133 | — |
| Product | HCID 86684927 | HCID 86684927 | — |
Reaction Steps
250 ml of pentadecylmagnesium bromide (15% in tetrahydroluran (THF); 119 mmol) are initially charged in a 1|4-neck flask with internal thermometer, argon blanketing, metal/water condenser and stirrer, and cooled to −30° C. Subsequently, a solution of 5.5 g (23.8 mmol) of 1,2-bis(dichlorophosphino)-ethane in 100 ml of THF is added dropwise within 30 minutes, in the course of which a large amount of solids precipitates. The mixture is then warmed to room temperature within one hour and subsequently stirred at internal temperature 50° C. for a further 2 hours, which gives rise to a grayish-white suspension. This is admixed gradually, and while cooling with ice, with 95 ml of saturated and degassed NH4Cl solution to obtain a white suspension. Another 65 ml of degassed water are added thereto and the precipitate is filtered off with suction through a G2 frit under argon. The product is washed once with water and twice with 20 ml of THF, and dried under reduced pressure. This gives 22.2 g (93.5%) of the product in the form of a white powder. 31P NMR (CDCl3): −26.8 ppm (s); elemental analysis: calc. C 79.6%, H 13.8%, P 6.6%; exp. C 79.5%, H 14.0%, P 6.3%, Br 0.04%, Cl 0.06%, O<0.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946462B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-cdec9ace95ba4ad096880116a5c5dfa5 |
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| Source note | uspto-grants-2015_02 |
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