Diisooctyl phthalate → Triphenylphosphine

HRID 1045037

反応式

HRID 1045037 の反応式
CC(CCCCCOC([C:12]1[C:17](C(OCCCCCC(C)C)=O)=[CH:16][CH:15]=[CH:14][CH:13]=1)=O)C.[CH:29]1[CH:30]=[CH:31][C:32]([P:35](C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)[C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=2)=[CH:33][CH:34]=1.C1OC2C(C3C4OCOC=4C=CC=3P(C3C=CC=CC=3)C3C=CC=CC=3)=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2O1.C1C2C=CC(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=2)CCC2C=CC(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=2)C1.COC1C(P(C2C=CC=CC=2)CCP(C2C(OC)=CC=CC=2)C2C=CC=CC=2)=CC=CC=1.CC(C(C)P(C1C=CC=CC=1)C1C=CC=CC=1)P(C1C=CC=CC=1)C1C=CC=CC=1.C1(P(CC2C(CP(C3C=CC=CC=3)C3C=CC=CC=3)OC(C)(C)O2)C2C=CC=CC=2)C=CC=CC=1.ClC1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=C(C2C(OC)=C(Cl)C=CC=2P(C2C=CC=CC=2)C2C=CC=CC=2)C=1OC.CC1P(C2C(P3C(C)CCC3C)=CC=CC=2)C(C)CC1.C1(P(C2C=CC=CC=2)C(CC(P(C2C=CC=CC=2)C2C=CC=CC=2)C)C)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C(P(C3C=CC=CC=3)C3C=CC=CC=3)CNC2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2CNC(CP(C3C=CC=CC=3)C3C=CC=CC=3)C2)C=CC=CC=1>>[CH:39]1[CH:38]=[CH:37][C:36]([P:35]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:32]2[CH:33]=[CH:34][CH:29]=[CH:30][CH:31]=2)=[CH:41][CH:40]=1

参加物

13

反応物 12

HCID 33934Diisooctyl phthalate2 回HCID 122582((5-((Diphenylphosphino)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl)(diphenyl)phosphineHCID 634876Binap, (A+-)-3 回HCID 27345571,2-Bis[(2-methoxyphenyl)phenylphosphino]ethane3 回HCID 3882352Chiraphos3 回HCID 41858942,4-Bis(diphenylphosphino)pentaneHCID 41875183,4-bis(diphenylphosphino)-PyrrolidineHCID 41893931,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzeneHCID 50000714-(diphenylphosphino)-2-[(diphenylphosphino)methyl]-PyrrolidineHCID 5165044(5,5'-Dichloro-6,6'-dimethoxy-2,2'-biphenyldiyl)bis(diphenylphosphine)HCID 10864772(R)-Phanephos2 回HCID 110175104,4'-Bi-1,3-benzodioxole-5,5'-diylbis(diphenylphosphine)3 回

生成物 1

HCID 11776Triphenylphosphine

実験手順

Synthesis of Complexes using C2 symmetric bis-P ligands (DIOP, BINAP, Cl-MeO-BIPHEP, SEGPHOS, PhanePHOS, DIPAMP, DuPHOS, BDPP, CHIRAPHOS, PPM, PYRPHOS) uses the compound [RuCl2(benzene)], RuCl2(PPh3)3 and trans-RuCl2(NBD)(py)2 as the starting material, while the complexes were prepared in accordance with the procedure published in the literature (Noyori, R.; Takeshi, O.; Hirohito, O. Shohei, H.; Takao, I. J. Am. Chem. Soc. 1995, 117, 2675; Akotsi, O. M.; Meters, K.; Reid, R. D.; McDonald, R.; Bergens, S. H. Chirality 2000, 12, 514-522; BINAP=2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, DIOP=4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane, Cl-MeO-BIPHEP=5,5′-Dichloro-6,6′-dimethoxy-2,2′-bis(diphenylphosphino)-1,1′-biphenyl, SEGPHOS=5,5′-Bis(diphenylphosphino)-4,4′-bi-1,3-benzodioxole, PhanePHOS=4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane, DIPAMP=1,2-Bis[(2-methoxyphenyl)(phenyl)phosphino]ethane, Me-DuPHOS=1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene, BDPP=2,4-Bis(diphenylphosphino)pentane, CHIRAPHOS=Bis(diphenylphosphino)butane, PYRPHOS=3,4-bis(diphenylphosphino)-Pyrrolidine, PPM=4-(diphenylphosphino)-2-[(diphenylphosphino)methyl]-Pyrrolidine. Synthesis of Complexes using C1 symmetric bis-P ligand (JosiPHOS, WalPHOS, MandyPHOS) uses the compound RuCl2(PPh3)3 as the starting material which can be obtained easily from hydrated RuCl3 and PPh3 (Steohenson, T. A.; Wilkinson, G. J. Inorg. Nucl. Chem. 1966, 28, 945-956; Josiphos=1-[Diarylphosphano]-2-[1-(dicyclohexylphosphano)ethyl]ferrocene.), while the complexes and RuCl2[(R,S)-Josiphos](PPh3) were prepared in accordance with the procedure published in the literature (Baratta, W.; Ballico, M.; Chelucci, G.; Siega, K.; Rigo, P. Angew. Chem. Int. Ed. 2008, 47, 4362-4365). The monochloride complex (11) was prepared from (10) by reacting with Et3N. The pre-catalysts used for in situ hydrogenation were [RuCl2BINAP(pyridine)2, RuCl2DIOP(pyridine)2, RuCl2(Josiphos)(pyridine)2]. As non-limiting examples of the present invention the synthesis and the characteristics of the complexes (8-25) are described in detail. All the syntheses were carried out under argon atmosphere, using freshly distilled solvents.

後処理

  1. customSynthesis of Complexes
  2. customwhile the complexes were prepared in accordance with the procedure
  3. customSynthesis of Complexes

出典と根拠

ORDレコード
ord-ee399126a4ea4fbb8e6c2d6923800d12
出典データセット
uspto-grants-2013_10
特許番号
US08563739B2

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