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Diisooctyl phthalate → Triphenylphosphine

HRID 1045037
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HRID 1045037 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

13

반응물 12

HCID 33934Diisooctyl phthalate2회HCID 122582((5-((Diphenylphosphino)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl)(diphenyl)phosphineHCID 634876Binap, (A+-)-3회HCID 27345571,2-Bis[(2-methoxyphenyl)phenylphosphino]ethane3회HCID 3882352Chiraphos3회
HCID 4185894
2,4-Bis(diphenylphosphino)pentane
HCID 41875183,4-bis(diphenylphosphino)-Pyrrolidine
HCID 41893931,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene
HCID 50000714-(diphenylphosphino)-2-[(diphenylphosphino)methyl]-Pyrrolidine
HCID 5165044(5,5'-Dichloro-6,6'-dimethoxy-2,2'-biphenyldiyl)bis(diphenylphosphine)
HCID 10864772(R)-Phanephos2회
HCID 110175104,4'-Bi-1,3-benzodioxole-5,5'-diylbis(diphenylphosphine)3회

생성물 1

HCID 11776Triphenylphosphine

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-ee399126a4ea4fbb8e6c2d6923800d12
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08563739B2

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