Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diphenylphosphinic chloride | HCID 73910 | — |
| Reactant | 5-Bromo-2-chloroanisole | HCID 2769567 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11078407 | HCID 11078407 | 82% |
Reaction Steps
Under argon, 1 mol of Mg turnings and a spatula tip of iodine in a mixture of 100 ml of tetrahydrofuran and 100 ml of toluene were heated to 60° C. Over the course of 10 minutes, 200 g of 5-bromo-2-chloroanisole in a mixture of 200 ml of tetrahydrofuran and 200 ml of toluene were added dropwise. During the dropwise addition, the internal temperature was maintained at 60° C. by cooling. When the dropwise addition was complete, the reaction mixture was heated to reflux temperature and after-stirred for 30 minutes at this temperature. The mixture was then cooled to 0° C. and 236.8 g of diphenylphosphinic chloride were added dropwise over the course of 45 minutes. The internal temperature was maintained during this operation between 0 and 5° C. The reaction mixture was after-stirred for 5 minutes at 0° C., the cooling was switched off, and the mixture was stirred for a further 2 hours. For work-up, the reaction mixture was poured onto 1.6 liter of iced water, the organic phase was separated off, and the aqueous phase was washed again with 2×400 ml of toluene. The combined organic phases were washed with 400 ml of 2.5% strength by weight aqueous soda solution and then with 400 ml of water, and then concentrated on a rotary evaporator to a volume of 200 ml. Then, with stirring, 300 ml of n-pentane were added dropwise. The solid that precipitated out overnight was filtered off with suction, washed with n-pentane, and dried. This gave 203.5 g of a white solid. The yield was 82% and the purity was 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489513B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-380af7ce6ce24665a0fead5b56cfc843 |
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| Source note | uspto-grants-2002_12 |
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