Process for production of phosphine derivative from phosphine oxide derivative
Disclosed is a process for producing a phosphine derivative from a phosphine oxide derivative, which comprises the following steps: (I) mixing a phosphine oxide derivative represented by formula (1) with a chlorinating agent in a polar organic solvent to cause the reaction between these components; and (II-1) adding a salt of a metal having an ionization tendency equal to or lower than that of aluminum to the reaction mixture and carrying out the reductive reaction in the presence of aluminum or (II-2) subjecting the reaction mixture to electrolytic reduction, thereby producing a phosphine derivative represented by formula (2). Ar n R 3-n P═O (1) Ar n R 3-n P (2) In formulae (1) and (2), Ar represents an aryl group such as a phenyl group, a phenyl group having a substituent, a heteroaromatic ring group, and a heteroaromatic ring group having a substituent; R represents an aliphatic hydrocarbon group or an aliphatic hydrocarbon group having a substituent; and n represents an integer of 0 to 3.
1. A method for producing Ar n R 3-n P from Ar n R 3-n P═O, comprising:
(I) mixing the Ar n R 3-n P═O with a chlorinating agent in a polar organic solvent, to cause a reaction; and
(II-1) adding a salt of a metal having an ionization tendency equal to or lower than that of aluminum to the reaction mixture, to carry out a reduction reaction in the presence of aluminum, or (II-2) subjecting the reaction mixture to electrolytic reduction,
and thereby producing the Ar n R 3-n P;
wherein Ar represents an aryl group; R represents an aliphatic hydrocarbon group or an aliphatic hydrocarbon group having a substituent; and n represents an integer of 0 to 3.
2. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and when adding the salt of a metal having an ionization tendency equal to or lower than that of aluminum, aluminum is also added to the reaction mixture.
3. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and when mixing the Ar n R 3-n P═O with the chlorinating agent in the polar organic solvent, aluminum is also mixed.
4. The method according to claim 1 , wherein the chlorinating agent is any one of oxalyl chloride, phosgene, diphosgene, and thionyl chloride.
5. The method according to claim 1 , wherein the Ar n R 3-n P═O is used in an amount of 5 to 50% by mass of the polar organic solvent.
6. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and aluminum is used in an amount of 0.66 to 5 mol based on 1 mol of the Ar n R 3-n P═O.
7. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and the salt of a metal is a salt of a metal having an ionization tendency equal to or lower than that of tin.
8. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and a chloride, a bromide, an iodide, a perchlorate, a sulfate, or a nitrate of a metal from groups 4 to 15 of the periodic table is used as the salt of a metal having an ionization tendency equal to or lower than that of aluminum.
9. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and the salt of a metal is a chloride or bromide of a metal having an ionization tendency equal to or lower than that of tin.
10. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and the salt of a metal having an ionization tendency equal to or lower than that of aluminum is used in an amount of 0.0001 to 1 mol based on 1 mol of aluminum.
11. The method according to claim 1 , wherein the polar organic solvent is an aprotic polar organic solvent.
12. The method according to claim 1 , wherein the polar organic solvent is acetonitrile or a mixed solvent comprising acetonitrile as a main solvent.
13. The method according to claim 1 , wherein the Ar n R 3-n P is produced by the reduction reaction in (II-1), and at that time, the reduction reaction is carried out in the presence of excess aluminum, and the Ar n R 3-n P═O, the chlorinating agent, and the polar organic solvent are further added to the aluminum collected after the reduction reaction, to produce the Ar n R 3-n P.
14. A method for producing Ar 3 P, comprising subjecting a mixture of Ar 3 P═O with a chlorinating agent to electrolytic reduction in a polar organic solvent;
wherein, Ar represents an aryl group.
15. A method for producing Ar 3 P from Ar 3 P═O, comprising:
mixing the Ar 3 P═O with a chlorinating agent in a polar organic solvent, to cause a reaction; and
adding a salt of a metal having an ionization tendency equal to or lower than that of aluminum to the reaction mixture to carry out a reduction reaction, thereby producing the Ar 3 P,
wherein the reduction reaction is carried out in the presence of aluminum;
and wherein Ar represents an aryl group.
16. The method according to claim 1 , wherein Ar is chosen from a phenyl group, a phenyl group having a substituent, a heteroaromatic ring group, and a heteroaromatic ring group having a substituent.
17. The method according to claim 14 , wherein Ar is chosen from a phenyl group, a phenyl group having a substituent, or a heteroaromatic ring group.
18. The method according to claim 17 , wherein Ar is a phenyl group having a substituent chosen from p-methyl and p-methoxy.
19. The method according to claim 17 , wherein Ar is a heteroaromatic ring group chosen from a 2-pyridyl group, a 3-pyridyl group, and a 3-thienyl group.
20. The method according to claim 15 , wherein Ar is chosen from a phenyl group, a phenyl group having a substituent, a heteroaromatic ring group, and a heteroaromatic ring group having a substituent.